Disease #01672 (EAOH (ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (EAOH)), OMIM:208920)
Official abbreviation |
EAOH |
Name |
ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia (EAOH) |
OMIM ID |
208920 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
59 |
Phenotype entries for this disease |
59 |
Associated with 1 gene |
APTX |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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