Disease #02413 (USH1F (Usher syndrome, type 1F (USH-1F)), OMIM:602083)

Official abbreviation USH1F
Name Usher syndrome, type 1F (USH-1F)
OMIM ID 602083
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene PCDH15
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00267037 patient PubMed: Vaché 2020, Journal: Vaché 2020 - F no France - - - - - USH1F - PCDH15 BICC1, LINC00844, PCDH15 3 1 David Baux
00413662 - - - - - Germany - - - - - USH1F - PCDH15 PCDH15 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00465320 - - - M no China - - - - - USH1F congenital bilateral hearing loss and first began to experience night blindness when the proband was about 10 years old PCDH15 PCDH15 1 2 Yanbao Xiang
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