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Results 1 - 10 of 35 for "OF-1"
  1. EYA1 gene 
    ... absent homolog 1 (Drosophila) eyes absent, Drosophila, homolog of, 1 Tests of EYA1 PubMed EYA TRANSCRIPTIONAL COACTIVATOR AND ...
    https://medlineplus.gov/genetics/gene/eya1 - Genetics
  2. Hypomyelination and congenital cataract 
    ... year of life. Development slows around the age of 1. Most affected children learn to walk between the ages of 1 and 2, although they usually need some type ...
    https://medlineplus.gov/.../hypomyelination-and-congenital-cataract - Genetics
  3. Spastic paraplegia type 2 
    ... brain. Symptoms usually become apparent between the ages of 1 and 5 years; those affected are typically able ...
    https://medlineplus.gov/genetics/condition/spastic-paraplegia-type-2 - Genetics
  4. Kallmann syndrome 
    ... males than in females, with an estimated prevalence of 1 in 30,000 males and 1 in 120, ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  5. Cerebrotendinous xanthomatosis 
    ... in the Moroccan Jewish population with an incidence of 1 in 108 individuals. Mutations in the CYP27A1 gene ...
    https://medlineplus.gov/.../condition/cerebrotendinous-xanthomatosis - Genetics
  6. Krabbe disease 
    ... the infantile form, usually begins before the age of 1. Initial signs and symptoms typically include irritability, muscle ...
    https://medlineplus.gov/genetics/condition/krabbe-disease - Genetics
  7. 3q29 microdeletion syndrome 
    ... from Iceland, the condition has an estimated incidence of 1 in 30,000 to 40,000 people in ...
    https://medlineplus.gov/.../condition/3q29-microdeletion-syndrome - Genetics
  8. Developmental and epileptic encephalopathy 1 
    ... spasms. The spasms usually appear before the age of 1. Several types of spasms have been described, but ...
    https://medlineplus.gov/...elopmental-and-epileptic-encephalopathy-1 - Genetics
  9. Hereditary neuralgic amyotrophy 
    ... episodes have occurred as early as the age of 1 year in some individuals. The attacks may be ...
    https://medlineplus.gov/.../hereditary-neuralgic-amyotrophy - Genetics
  10. HSD10 disease 
    ... This developmental regression often occurs between the ages of 1 and 2 and results in severe intellectual disability ...
    https://medlineplus.gov/genetics/condition/hsd10-disease - Genetics
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