Disease #00669 (USH2C (Usher syndrome,, type IIC (USH2C, GPR98/PDZD7 digenic)), OMIM:605472)

Official abbreviation USH2C
Name Usher syndrome,, type IIC (USH2C, GPR98/PDZD7 digenic)
OMIM ID 605472
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive, Digenic dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 2 genes GPR98, PDZD7
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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00361902 - - - - - - - - - - - albinism, USH2C Deafness, blurring of vision, generalised hypopigmentation, light coloured iris - GPR98, TYR 2 1 Anju Shukla
00436543 2480223 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M no Mexico Hispanic - - - NONE USH2C Reduced visual acuity HP:0007663, Nyctalopia HP:0000662, Peripheral visual field loss HP:0007994, Retinitis pigmentosa HP:0000510, Moderate sensorineural hearing impairment HP:0008504 USH1C USH1C 2 1 Rocio Villafuerte-de la Cruz
00464547 - - - F yes Israel Muslim Arab - - - - ID, skeletal dysplasia, USH2C - - GPR98, SMARCA2 2 1 Tamar Ben-Yosef
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