Disease #00481 (OCA4 (albinism, oculocutaneous, type IV (OCA-4)), OMIM:606574)

Official abbreviation OCA4
Name albinism, oculocutaneous, type IV (OCA-4)
OMIM ID 606574
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene SLC45A2
Associated tissues -
Disease features -
Remarks -
Date created 2014-07-24 22:24:28 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00164363 - - - - - - - - - - - OCA4 - SLC45A2 SLC45A2 2 1 Gemeinschaftspraxis für Humangenetik Dresden
00435574 - - - - - India - - - - - OCA4 - SLC45A2 SLC45A2 1 1 Sudha Kohli, Renu Saxena, Ratna Puri, I.C. Verma
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