Disease #03762 (USH1J (Usher syndrome, type 1J (USH1J)), OMIM:614869)

Official abbreviation USH1J
Name Usher syndrome, type 1J (USH1J)
OMIM ID 614869
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CIB2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-11-11 09:54:40 +01:00 (CET)


Individuals

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00029793 FamPKDF117 PubMed: Riazuddin 2012, Journal: Riazuddin 2012 6-generation family, 4 affecteds (1F, 3M), unaffected carrier parents - yes Pakistan - - - - - USH1J see paper CIB2 CIB2 1 4 Johan den Dunnen
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