Disease #00479 (OCA3 (albinism, oculocutaneous, type III (OCA-3)), OMIM:203290)
Official abbreviation |
OCA3 |
Name |
albinism, oculocutaneous, type III (OCA-3) |
OMIM ID |
203290 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
9 |
Phenotype entries for this disease |
7 |
Associated with 1 gene |
TYRP1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-07-24 22:04:08 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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