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

9 entries on 1 page. Showing entries 1 - 9.
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00117461 - - - - - Germany - - - - - OCA3 - TYRP1 TYRP1 2 1 Gemeinschaftspraxis für Humangenetik Dresden
00204366 - - - - - - white - - - - OCA3 - TYRP1 TYRP1 1 1 William (Bill) Oetting
00204367 - - - - - - - - - - - OCA3 - TYRP1 TYRP1 1 1 William (Bill) Oetting
00204369 - - - - - - - - - - - OCA3 - TYRP1 TYRP1 1 1 William (Bill) Oetting
00204370 - - - - - India Asian - - - - OCA3 - TYRP1 TYRP1 1 1 William (Bill) Oetting
00204374 - - - - - - - - - - - OCA3 - TYRP1 TYRP1 1 1 William (Bill) Oetting
00204375 - - - - - - white - - - - OCA3 - TYRP1 TYRP1 1 1 William (Bill) Oetting
00295533 - - - - - - - - - - - OCA3 - TYRP1 TYRP1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00435575 - - - ? - - - - - - - OCA3 - TYRP1 TYRP1 1 1 Sudha Kohli, Renu Saxena, Ratna Puri, I.C. Verma
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