Phenotypes for disease #00115 (INAD (Infantile Neuroaxonal Dystrophy), OMIM:256600)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Inheritance     

Owner     

Individual ID     
0000000209 developmental regression starting from the age of 1 year 5 months, bilateral convergent strabismus, central hypotonia, dystonia, tremors, generalized hyper-reflexia and extensor plantar responses, bilateral optic atrophy - Nur Aisyah Athirah 00000597
0000000210 auditory neuropathy - Nur Aisyah Athirah 00000598
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