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Symptom Checker » Anteverted nostrils » Long thin fingers
 

Anteverted nostrils and Long thin fingers and Night blindness and Skin texture changes and Spasms and Tooth deformity
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Anteverted nostrils and Long thin fingers and Night blindness and Skin texture changes and Spasms and Tooth deformity

  • Anteverted nostrils AND Long thin fingers AND Night blindness AND Skin texture changes AND Spasms AND Tooth deformity - Causes of All Symptoms
  • Anteverted nostrils OR Long thin fingers OR Night blindness OR Skin texture changes OR Spasms OR Tooth deformity - 2897 causes

Anteverted nostrils:

Long thin fingers:

Night blindness:

Skin texture changes:

Spasms:

Tooth deformity:

Results: Causes of Anteverted nostrils AND Long thin fingers AND Night blindness AND Skin texture changes AND Spasms AND Tooth deformity

Results: 2897 causes of Anteverted nostrils OR Long thin fingers OR Night blindness OR Skin texture changes OR Spasms OR Tooth deformity

    1. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    2. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    3. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    4. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    5. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    6. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    7. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    8. 3 alpha methylglutaconicaciduria, type 3
     A rare genetic condition where a gene mutation prevents the production of certain protein which leads to a build-up of an acid (3-methylglutaconic acid) which can have a negative impact on the body. The condition is characterized mainly by damage to the o...more »
    9. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    10. 3-Hydroxyisobutyric aciduria
     A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems....more »

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