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Symptom Checker » Cellulitis » Excess skin pigmentation
 

Cellulitis and Excess skin pigmentation
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Results: Causes of Cellulitis AND Excess skin pigmentation

    1. Eczema
     Eczema is a chronic skin condition characterized by skin inflammation and irritation. The severity of extent of the condition is highly variable. It may be caused by allergies, irritants or other factors such as stress....read more »

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Note: Do not use for diagnosis; see limitations of results.

Results: 158 causes of Cellulitis OR Excess skin pigmentation

    1. ACTH resistance
     A rare inherited genetic disorder characterized by adrenal insufficiency due to the adrenal gland's inability to respond to ACTH and hence produce the hormone called cortisol....more »
    2. APECED Syndrome
     APECED is a recessively inherited genetic disease characterized by the presence of two of the following three conditions: impaired parathyroid function, yeast infection (candidiasis) and impaired adrenal gland function (Addison's disease). It is an autoim...more »
    3. Aagenaes syndrome
     A rare inherited birth abnormality involving underdeveloped lymph vessels which results in swollen legs and liver problems....more »
    4. Acanthosis nigricans
     It is a brown to black, poorly defined, velvety hyperpigmentation of the skin usually present in the posterior and lateral folds of the neck, the axilla, groin, umbilicus and other areas....more »
    5. Achalasia -- Addisonianism -- Alacrimia syndrome
     A rare inherited disorder characterized mainly by achalasia, alacrimia (absent tears) and Addison's disease. Addison's disease involves adrenal insufficiency due to a resistance to adrenocorticotropic hormone. Only about 70 cases reported worldwide....more »
    6. Achalasia -- addisonianism -- alacrima syndrome
     A rare inherited disorder characterized mainly by achalasia, alacrimia (absent tears) and Addison's disease. Addison's disease involves adrenal insufficiency due to a resistance to adrenocorticotropic hormone. Only about 70 cases reported worldwide....more »
    7. Achalasia -- adrenal -- alacrima syndrome
     A familial disorder characterized by adrenal gland-related hormonal problems, swallowing difficulty (achalasia) and a lack of tears (alacrima). Neurological impairment and motor and sensory neuropathy is progressive. The adrenal glands in patients are res...more »
    8. Acne
     Pimples and blackheads on the face and skin....more »
    9. Addison's Disease
     A rare progressive hormonal disorder characterized by insufficient production of certain hormones called adrenal corticosteroids....more »
    10. Adenitis
     Inflammation of a lymph gland...more »
    11. Adrenal gland hypofunction
     Reduced adrenal gland activity due to damage to the adrenal gland or lack of stimulation of the gland. Pituitary hormones stimulate adrenal gland activity....more »
    12. Adrenal hyperplasia
     A group of disorder that occur when there is a problem in the process of making adrenal corticosteroids....more »
    13. Adrenal hyperplasia, congenital type 3
     A group of disorders that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The severity of the condition is variable depending on the degree of deficiency....more »
    14. Adrenal hypofunction
     A condition which is characterized by a lack of production of hormones from the adrenal gland....more »
    15. Adrenal hypoplasia congenital, X-linked
     A genetic disorder which affects the body tissues that produce hormones. It is characterized by underdeveloped adrenal glands which results adrenal insufficiency and hypogonadotrophic hypogonadism....more »
    16. Adrenoleukodystrophy
     A rare disorder which has characteristic symptoms of Addison disease (adrenocortical insufficiency) and Schilder disease (cerebral sclerosis). Bronze skin, brain sclerosis and demyelination are the main symptoms....more »
    17. Alcohol-induced pseudo-Cushing syndrome
     The excessive consumption of alcohol can result in symptoms similar to a condition called Cushing's syndrome. When alcohol consumption is stopped, symptoms regress....more »
    18. Alkaptonuria
     A rare disorder where the abnormal accumulation of a particular acid (homogentisic acid) in the body causes connective tissue and bone damage. This damage gives tissues a dark or bluish discoloration....more »
    19. Angioma
     Clump of blood or lymph vessels usually in the skin...more »
    20. Aplasia cutis congenita -- epibulbar dermoids
     A very rare syndrome characterized by increased skin pigmentation, a localized absence of skin (aplasia cutis congenital) and epibulbar dermoids (a benign eye tumor)....more »
    21. Bacterial diseases
     Diseases caused by a bacterial infection...more »
    22. Bamforth syndrome
     A rare syndrome characterized mainly by the association of an abnormal opening in the roof of the mouth and reduced thyroid functioning....more »
    23. Becker's nevus
     A rare skin disorder where an irregular pigmented patch on the skin slowly grows and becomes thick and hairy....more »
    24. Berardinelli-Seip congenital lipodystrophy
     A rare genetic disorder characterized by diabetes mellitus, loss of body fat, hepatomegaly, enlarged genitals, increased skeletal growth and other abnormalities....more »
    25. Berardinelli-Seip congenital lipodystrophy, type 1
     A rare genetic disorder characterized by early-onset diabetes mellitus, loss of body fat, serious insulin resistance, high blood triglycerides and fatty liver. Type 1 is distinguished from type 2 by the origin of the genetic defect. Type 1 is caused by a ...more »
    26. Berardinelli-Seip congenital lipodystrophy, type 2
     A rare genetic disorder characterized by early-onset diabetes mellitus, loss of body fat, serious insulin resistance, high blood triglycerides and fatty liver. Type 2 is distinguished from type 2 by the origin of the genetic defect. Type 2 is caused by a ...more »
    27. Birthmark
     Skin marking appearing from birth...more »
    28. Brachioradial pruritus
     A condition characterized by itching, burning and other sensations of the skin on one or both arms. The skin has no visible evidence of the skin unless the patient causes damage to the skin due to scratching or rubbing. The condition results from nerve da...more »
    29. Bullous Pemphigoid
     A chronic skin disorder characterized blistering of the skin which usually occurs on the joints, abdomen, armpit and groin areas....more »
    30. Cardiofaciocutaneous Syndrome
     A rare genetic disorder characterized by short stature, congenital heart defects skin anomalies and frontal bossing....more »
    31. Carney syndrome
     A very rare syndrome characterized by spotty pigmentation on the skin and the development of multiple benign tumors (myxoma) that can occur just about anywhere in the body but mainly in the skin, breast and heart and endocrine glands such as the thyroid a...more »
    32. Carotenemia, familial
     A rare inherited metabolic disorder where an enzyme deficiency inhibits the conversion of beta carotene into vitamin A. Thus, patients have high beta carotene levels in the blood and low vitamin A levels. The condition causes intermittent orange discolora...more »
    33. Chediak-Higashi Syndrome
     An inherited immune system disorder characterized by reduced pigmentation, recurrent infection and neurological disorders....more »
    34. Chemical poisoning -- Paraffin wax
     Paraffin wax is a chemical used mainly in the production of candles, paraffin papers, varnishes, floor polishes, food packaging, lubricants, cosmetics, wood waterproofing, cork and perfume extraction. The fumes from burning paraffin wax can be quite harmf...more »
    35. Chemical poisoning -- Silver
     Silver is a chemical used mainly in electric products and photography. Ingestion and other exposures to the chemical can cause various symptoms. The type and severity of symptoms varies depending on the amount of chemical involved and the nature of the ex...more »
    36. Chloasma
     Red facial marks in women related to hormones...more »
    37. Chromosome 14 trisomy
     A rare chromosomal disorder involving duplication of genetic material from chromosome 14 resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is duplicated....more »
    38. Chromosome 14 trisomy syndrome
     A rare chromosomal disorder involving duplication of genetic material from chromosome 14 resulting in various abnormalities....more »
    39. Chromosome 14q deletion syndrome
     A rare chromosomal disorder involving deletion of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    40. Chronic Kidney Disease
     Long-term and generally irreversible disease of the kidneys due to infection, obstruction, congenital diseases or generalised diseases causing failure of the kidneys' normal functions....more »
    41. Classic childhood ALD
     Classic severe form of ALD in boys....more »
    42. Clostridium perfringens food poisoning
     Common type of food poisoning....more »
    43. Congenital Lipomatous Overgrowth, Vascular Malformations and Epidermal Nevi
     A rare syndrome characterized by overgrowth of fatty tissue, blood vessel malformations and skin birth marks. The condition is a progressive one and there have been less than 20 reported cases....more »
    44. Congenital Lipomatous Overgrowth, Vascular Malformations, Epidermal Nevi, and Skeletal/Spinal abnormalities
     A rare syndrome characterized by overgrowth of fatty tissue, blood vessel malformations, birth marks and skeletal and spinal abnormalities. The condition is a progressive one and there have been less than 20 reported cases....more »
    45. Congenital adrenal hyperplasia (CAH)
     A group of disorder that occur when there is a problem in the process of making adrenal corticosteroids....more »
    46. Congenital adrenal hyperplasia -- simple virilizing form in males
     A group of disorder that occur when a deficiency of 21-hydroxylase impairs the normal process of making adrenal corticosteroids. The simple virilizing form involves a moderate deficiency of 21-hydroxylase and differs in its effects on males and females....more »
    47. Craniolenticulosutural dysplasia
     A rare syndrome characterized by skeletal defects and an unusual facial appearance consisting mainly of a prominent forehead, wide-set eyes, broad nose and a prominent forehead with a birthmark....more »
    48. Cushing's disease
    49. Cushing's syndrome
     A rare syndrome where excessive secretion of corticosteroids by the adrenal cortex leads to a variety of symptoms. Hormone-secreting adrenal or pituitary tumors are often the cause of the excessive corticosteroid secretion....more »
    50. Cutaneomeningospinal angiomatosis
     A rare inherited disorder involving a skin birthmark as well as a blood vessel malformation in the spinal cord (angioma). The severity of the spinal involvement is variable with neurological problems occurring as a result of compression of the spinal cord...more »
    51. Cyclophosphamide -- Teratogenic Agent
     There is evidence to indicate that exposure to Cyclophosphamide during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of ex...more »
    52. Dermatofibroma
     A benign skin growth that usually occurs on the legs but may affect the arms or trunk. The growth is usually discolored and contains hard, scar-like tissue. A minor injury such as an insect bite or a thorn can result in a dermatofibroma. The color of the ...more »
    53. Dermatopathia pigmentosa reticularis
     A very rare syndrome characterized mainly by increased skin pigmentation, thickened skin on palms and soles and reduced sweating....more »
    54. Diabetes
     Failing or reduced ability of the body to handle sugars....more »
    55. Dowling-Degos disease
     A rare condition characterized by progressive enlargement of pigmented areas that occur on areas of creased or folded skin such as armpits, groin, breasts and limbs....more »
    56. Duhring disease
     A rare chronic skin disorder involving rashes of small skin bumps and blisters that are extremely itchy....more »
    57. Dyck Syndrome
     A very rare condition observe in two brothers. It involves vision, hearing, muscle, sensory and adrenal system problems and an enlarged liver and spleen....more »
    58. Dyschromatosis symmetrica hereditaria 1
     A very rare syndrome characterized mainly by patches of abnormal skin pigmentation affecting the face and back of hands and top of feet....more »
    59. Dyskeratosis Congenita
     A rare genetic disorder characterized by sking pigmentation abnormalities, nail dystrophy and mucous membrane changes....more »
    60. Eczema
     Eczema is a chronic skin condition characterized by skin inflammation and irritation. The severity of extent of the condition is highly variable. It may be caused by allergies, irritants or other factors such as stress....more »
    61. Elderly conditions
     Any of the conditions affecting the elderly....more »
    62. Erythema ab igne
    63. Fanconi's anemia
     Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and ot...more »
    64. Gaucher Disease
     A rare inherited biochemical disorder characterized by the deficiency of the enzyme called glucocerebrosidase and accumulation of glycosylceramide (glucocerebroside). There are three forms of this disease: type 1, 2 and 3....more »
    65. Gravitational eczema
     Gravitational eczema is a chronic skin condition that affects the lower legs and is caused by problems with the veins in the legs e.g. blood clots or varicose veins....more »
    66. HIV/AIDS
     HIV is a sexually transmitted virus and AIDS is the progressive immune failure that HIV causes....more »
    67. Hay-Wells Syndrome
     A rare genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate....more »
    68. Hay-Wells syndrome, recessive type
     A rare recessively inherited genetic disorder characterized by ankyloblepharon, ectodermal dysplasia, and cleft lip and/or cleft palate. The recessive form of this condition is distinguished by the presence at birth of adhesions between the upper and lowe...more »
    69. Hemochromatosis
     Excess of iron leading to problems with joints, liver, heart and pancreas....more »
    70. Hemophilus influenzae B
     Bacterial respiratory infection with dangerous complications....more »
    71. Hereditary Hemochromatosis
     A genetic disorder where too much iron is absorbed from food and it is stored in various parts of the body which can cause damage. There are 4 types of hemochromatosis and they are distinguished by age of onset, genetic cause and type of inheritance. Some...more »
    72. Human carcinogen -- Busulphan
     Busulphan is deemed to be carcinogenic to humans. The carcinogenicity of the substance may be influenced by the duration and level of exposure....more »
    73. Humeroradioulnar synostosis
     A very rare syndrome characterized mainly by abnormalities in the arm bones where some of the bones in the upper and lower arms are fused....more »
    74. Hyperpigmentation
    75. Hyperpigmentation, Cutaneous, With Hypertrichosis, Hepatosplenomegaly, Heart Anomalies, Hearing Loss, And Hypogonadism
     A rare syndrome characterized by various skin and nail anomalies as well as other problems....more »
    76. Hypoadrenalism
     Reduced adrenal gland activity....more »
    77. Hypomelanosis of Ito
     A rare genetic neurocutaneous disorder characterized by unusual patterns of depigmented skin and associated disorders such as seizures, psychomotor retardation and eye abnormalities....more »
    78. Incontinentia Pigmenti
     A rare genetic skin pigmentation disorder characterized by eye, teeth, bone, nail and hair malformations as well as central nervous abnormalities and mental deficiency....more »
    79. Jaundice
     Bile or liver problem causing yellowness....more »
    80. Kwashiorkor
     A malnutrition state that is produced by severe protein deficiency...more »
    81. LEOPARD Syndrome
     A rare genetic disorder characterized by multiple lentigines, pulmonic stenosis, widely spaced eyes and deafness....more »
    82. Laugier-Hunziker syndrome
     A rare skin abnormality involving flat pigmentated patches of skin on the lips and inside mouth as well as black streaky lines on the nails....more »
    83. Lichen planus
     Skin rash...more »
    84. Lipoid congenital adrenal hyperplasia
     A rare form of congenital adrenal hyperplasia where the early phase of adrenal cortisol production is defective which causes mineralocorticoid deficiency. Male pseudohermaphroditism is the main characteristic of this disorder....more »
    85. Lupus
     Autoimmune disease with numerous effects on various organs and linings....more »
    86. Lymphatic Obstruction
     A blockage of the lymph vessels that drain fluid from body tissues and facilitate immune system cell movement through the body. Lymphatic obstruction can be caused by such things as tumors, surgery, injury and infection. Obstruction can be primary (as in ...more »
    87. Lymphocytic vasculitis
     Blood vessel inflammation due to infiltration of blood vessel walls with lymphocytes which can causes raised skin welts which can be tender and painful. The skin often remains darkened after the lesions are resolved....more »
    88. Macular amyloidosis
     A skin condition caused by abnormal deposits of amyloid in the skin. Skin lesions usually occur on the chest, between the shoulder blades and sometimes the arms....more »
    89. Mastocytosis
     A disorder where excessive amounts of mast cells proliferate in organs such as the skin, liver, bone, spleen and gastrointestinal tract. Mast cells occur in connective tissue and defend the body against disease by releasing histamine to stimulate the immu...more »
    90. McCune-Albright Syndrome
     A rare genetic multisystem disorder characterized by abnormal skin pigmentation and endocrine gland dysfunction and replacement of parts of bone tissue with fibrous material....more »
    91. Melanoma
     Melanoma is the most dangerous type of skin cancer. It is the leading cause of death from skin disease. It involves cells called melanocytes, which produce a skin pigment called melanin. Melanin is responsible for skin and hair color....more »
    92. Mental retardation -- hypotonia -- skin hyperpigmentation
     A rare condition characterized mainly by mental retardation, reduced muscle tone and increased skin pigmentation....more »
    93. Minocycline -- Teratogenic Agent
     There is evidence to indicate that exposure to Minocycline during pregnancy may have a teratogenic effect on the fetus. A teratogen is a substance that can cause birth defects. The likelihood and severity of defects may be affected by the level of exposur...more »
    94. Mole
     Darkened growths on the skin; everyone has a few....more »
    95. Naegeli syndrome
     An inherited skin disorder characterized by reticulated pigmentation on the skin. The skin on palms and soles may thicken and ability to sweat may be reduced....more »
    96. Needlefish bite
     The Needlefish is long-beaked surface fish found in tropical and sub-tropical oceans. The needlefish can deliver a serious bite but has no venom. These fish are attracted to bright lights and can propel themselves out of the water towards the light source...more »
    97. Nelson Syndrome
     The rapid growth of a pituitary adenoma (tumor) after the surgical removal of both adrenal glands to treat Cushing's disease. The condition is triggered by the resultant loss of the regulatory function of cortisol....more »
    98. Nephrogenic Fibrosing Dermopathy
     A rare disorder characterized by thickening and hardening of the skin as well as other symptoms. The course of the disease may be mild or aggressive and occurs in patients with underlying disorders kidney disease....more »
    99. Neurodermatitis
     Lichen simplex chronicus refers to thickened itchy skin that results from persistently rubbing or scratching an area of skin....more »
    100. Neurofibromatosis
     Nerve disorders often leading to tumors on nerves....more »
    101. Nevus flammeus
     A condition which is characterized by any congenital skin lesion...more »
    102. Nevus of Ota
     A very rare syndrome characterized by abnormal pigmentation of the eye and the skin surrounding the eye. Usually only one eye is affects and the discoloration often follows the distribution of the trigeminal nerve....more »
    103. Nocardiosis
     A rare infectious disease caused by the bacteria Nocardia asteroides which primarily affects the lung but may also involve the brain, soft tissues and other organs....more »
    104. POEMS
     A very rare disorder that has widespread effects on the body: P -- polyneuropathy, O -- organopathy, E -- endocrinopathy, M -- monoclonal gammopathy and S -- skin changes....more »
    105. POEMS syndrome
     A very rare disorder that has widespread effects on the body: P - polyneuropathy, O - organopathy, E - endocrinopathy, M - monoclonal gammopathy, S - skin changes....more »
    106. Parry Romberg Syndrome
     Wasting away of one side of the face....more »
    107. Pasteurella multocida
     An infectious disease caused by a bacterium called Pasteurella multocida. It is often transmitted through bites and scratches from pets and it can be found in mammals and fowl....more »
    108. Periorbital Cellulitis
     Bacterial infection of the superficial tissues surrounding the eyes, often following a conjunctivitis or middle ear infection...more »
    109. Peripheral vascular disease
     Disease of arteries supplying the legs or sometimes arms...more »
    110. Peutz-Jeghers Syndrome
     A rare genetic disorder characterized by the development of numerous benign nodules on the inside lining of the intestinal wall as well as excess skin pigmentation usually around the lips and inner lining of the mouth....more »
    111. Phototoxic eczema
     Phototoxic eczema is skin irritation and inflammation which occurs as an abnormal response to exposure to UV light radiation. The cause of this sensitivity may result from the use of certain drugs or exposure various other photosensitizing substances such...more »
    112. Poikiloderma of Rothmund-Thomson
     A rare disease which causes sufferers to have a senile-like appearance with skin, growth, hair and eye abnormalities....more »
    113. Polycystic ovary syndrome
     Polycystic ovary syndrome (PCOS) is an endocrine disorder that affects approximately 5% of all women....more »
    114. Porphyria cutanea tarda, sporadic type
     A rare metabolic condition involving a deficiency of the enzyme uroporphyrinogen decarboxylase in the liver only. Type II involves a deficiency of the same enzymes activity in various tissues throughout the body....more »
    115. Possible human carcinogenic exposure -- Bleomycin
     Some evidence indicates that exposure to Bleomycin has a possible link to an increased risk of developing cancer in humans. The carcinogenicity of the substance may be influenced by the duration and level of exposure. Bleomycin is used primarily as a chem...more »
    116. Pregnancy
     The condition of supporting a fetus from conception till birth....more »
    117. Primary Biliary Cirrhosis 1
     Primary biliary cirrhosis is a chronic condition involving progressive destruction of the bile ducts in the liver. This results in an abnormal buildup of bile in the liver which eventually progresses to liver failure. Primary biliary cirrhosis 1 is linked...more »
    118. Primary Biliary Cirrhosis 2
     Primary biliary cirrhosis is a chronic condition involving progressive destruction of the bile ducts in the liver. This results in an abnormal buildup of bile in the liver which eventually progresses to liver failure. Primary biliary cirrhosis 2 is linked...more »
    119. Primary Biliary Cirrhosis 3
     Primary biliary cirrhosis is a chronic condition involving progressive destruction of the bile ducts in the liver. This results in an abnormal buildup of bile in the liver which eventually progresses to liver failure. Primary biliary cirrhosis 3 is linked...more »
    120. Primary Lymphatic Obstruction
     A blockage of the lymph vessels from birth. Lymph vessels drain fluid from body tissues and facilitate immune cell movement through the body. Primary obstruction can be the result of underdeveloped or malformed lymph vessels....more »
    121. Primary biliary cirrhosis
     Primary biliary cirrhosis is a chronic and progressive cholestatic disease of the liver....more »
    122. Proteus Syndrome
     A rare genetic disorder characterized by overgrowth of bones, fatty tissues and skin in various parts of the body....more »
    123. Prurigo
     Itchy nodules created by repeated scratching....more »
    124. Prurigo nodularis of Hyde
     A relatively uncommon skin disorder involving the development of firm itchy skin nodules. The nodules usually start on the arms and legs but can affect any part of the body in varying numbers. The exact cause is unknown but it is often associated with con...more »
    125. Psoriasis
     Psoriasis is an inflammatory skin condition where the defective immune system causes skin cells to grow rapidly. It affects a significant number of people. Arthritis, which can be severe, is associated with the psoriasis in up to a third of cases. Not all...more »
    126. Revesz Syndrome
     A very rare syndrome characterized mainly by disease of the eye retinas, anemia and central nervous system anomalies....more »
    127. River Blindness
     Skin and eye infection caused by the helminth (worm) 'Onchocerca volvulus', transmitted via fly bites and usually seen only in parts of Africa, the Middle East and South America...more »
    128. Rokitansky Van Bogaert syndrome
     A rare disorder characterized by pigmentation abnormalities of the skin and brain which causes various neurological symptoms as well as skin nevi....more »
    129. Saul-Wilkes-Stevenson syndrome
     A very rare syndrome characterized mainly by muscle problems, abnormal skin pigmentation, movement disorder, mental retardation and scoliosis....more »
    130. Schwartz newark syndrome
     A rare syndrome characterized by pigmentation anomaly, hydrocephaly, spina bifida and a myelomeningocele....more »
    131. Schwartz, Cohen-Addad, Lambert syndrome
     A rare disorder characterized by increased pigmentation and a central nervous system malformation (myelomeningocele)....more »
    132. Scleredema adultorum
     A rare skin condition characterized by thickening of the skin usually in the head, neck and upper body area. The disorder is often associated with conditions such as infections, myelomas and diabetes....more »
    133. Scleroderma
     A rare, progressive connective tissue disorder involving thickening and hardening of the skin and connective tissue. There are a number of forms of scleroderma with some forms being systemic (involving internal organs)....more »
    134. Scleroderma, systemic
     A rare autoimmune connective tissue disease where the body attacks parts of the body and causes scarring and thickness of the tissue. In the systemic form, the skin and organs are involved....more »
    135. Secondary Lymphatic Obstruction
     A blockage of the lymph vessels that occurs secondary to some other condition such as infection. Lymph vessels drain fluid from body tissues and facilitate immune cell movement through the body. Secondary lymphatic obstruction can be caused by such things...more »
    136. Sezary syndrome
     A rare type of lymphoma characterized by skin redness, leukemia and enlarged lymph nodes....more »
    137. Short limbs subluxed knees cleft palate
     A rare syndrome characterized mainly by short limbs, partially dislocated knees and a cleft palate....more »
    138. Sparse hair -- short stature -- skin anomalies
     A rare syndrome characterized mainly by sparse hair, short stature and skin anomalies....more »
    139. Spastic paraplegia 23
     A rare disorder characterized mainly by progressive stiffness and weakness of the leg muscles, premature graying, characteristic facial appearance and a skin pigmentation anomaly. Pigmentation anomalies usually start from the age of 6 months and leg probl...more »
    140. Spondyloepiphyseal dysplasia -- nephrotic syndrome
     A very rare syndrome characterized by skeletal and immunity abnormalities. The immune defect leads to progressive kidney dysfunction which can ultimately cause death during the first decade....more »
    141. Spondylohypoplasia arthrogryposis popliteal pterygium
     A very rare inherited syndrome characterized by webbing at the back of the knees, spinal defects and various other skeletal abnormalities....more »
    142. Spondylohypoplasia, arthrogryposis and popliteal pterygium
     A very rare inherited syndrome characterized by webbing at the back of the knees, spinal defects and various other skeletal abnormalities....more »
    143. Staphylococcal infection
     Any infection caused by the bacteria staphylococcal...more »
    144. Stomach cancer
     Stomach or gastric cancer can develop in any part of the stomach and may spread throughout the stomach and to other organs...more »
    145. Streptococcal Infections
     Various "strep" bacterial infections....more »
    146. Tang Hsi Ryu syndrome
     A rare syndrome characterized by enlarged liver and spleen, increased pigmentation and abnormal peripheral nerve functioning....more »
    147. Tinea
     A general term for various fungal skin afflictions; often incorrectly called ringworm....more »
    148. Tinea versicolor
     A condition which is characterized by a chronic noninflammatory multiple macular patches...more »
    149. Varicose veins
     Enlarged blue veins, usually in the legs....more »
    150. Variegate porphyria
     A rare metabolic disorder characterized by a deficiency of a certain enzyme which results in a build-up in the body of porphyrins or their precursors. This form of hepatic porphyria causes the sufferer to have acute attacks as well as skin sensitivity....more »
    151. Visceral leishmaniasis
     A condition which is characterized by an infection of the viscera by leishmaniasis...more »
    152. Vitreoretinochoroidopathy dominant
     A form of hereditary fundus dystrophy...more »
    153. WHIM syndrome
     A rare syndrome characterized by warts, hypogammaglobulinemia (low blood gammaglobulin levels), recurring bacterial infections and myelokathexis (form of neutropenia). It is a form of immunodeficiency disease caused by a mutation in a chemokine receptor....more »
    154. Whipple's Disease
     Rare malabsorption disease from bacterial digestive infection...more »
    155. Whyte Murphy Syndrome
     A syndrome which is characterised by hyperpigmentation, white forelock and osteopathia striata...more »
    156. Wolcott-Rallison syndrome
     A very rare genetic condition characterized primarily by the onset of diabetes mellitus during infancy and epiphyseal dysplasia (abnormal joint development)....more »
    157. Yemenite deaf-blind hypopigmentation syndrome
     A condition which is characterised by the association of several symptoms which affect ones hearing and vision...more »
    158. Zellweger-like syndrome, without peroxisomal anomalies
     A rare syndrome characterized by unusual facial appearance, very low muscle tone, mental retardation and metabolic defects....more »

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