Disease #00485 (OA1 (albinism, ocular, type I (OA-1,Nettleship-Falls type)), OMIM:300500)

Official abbreviation OA1
Name albinism, ocular, type I (OA-1,Nettleship-Falls type)
OMIM ID 300500
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease 9
Phenotype entries for this disease 7
Associated with 1 gene GPR143
Associated tissues eyes
Disease features -
Remarks -
Date created 2014-07-24 23:05:27 +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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00080700 - - - M - Germany - - - - - OA1 no cutaneous involvement GPR143 GPR143 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00105018 81ORG1 PubMed: de Castro-Miró 2016 - F no Argentina - - - - - OA1 - - OPA1 1 1 Marta de Castro-Miró
00384252 13169 PubMed: Wang 2019 - M - China - - - - - OA1 - GPR143 GPR143 1 1 LOVD
00384267 13302 PubMed: Wang 2019 - M - China - - - - - OA1 - GPR143 GPR143 1 1 LOVD
00384298 13518 PubMed: Wang 2019 - M - China - - - - - OA1 - GPR143 GPR143 1 1 LOVD
00384398 14216 PubMed: Wang 2019 - M - China - - - - - OA1 - GPR143 GPR143 1 1 LOVD
00384415 14395 PubMed: Wang 2019 - M - China - - - - - OA1 - GPR143 GPR143 1 1 LOVD
00435573 - - - M - India - - - - - OA1 - GPR143 GPR143 1 1 Sudha Kohli, Renu Saxena, Ratna Puri, I.C. Verma
00436788 alb0052 - - - - India indian - - - - OA1 - - GPR143 1 1 Sudha Kohli, Renu Saxena, Ratna Puri, I.C. Verma
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