Disease #03596 (WFSL (Wolfram-like syndrome, autosomal dominant (WFSL)), OMIM:614296)

Official abbreviation WFSL
Name Wolfram-like syndrome, autosomal dominant (WFSL)
OMIM ID 614296
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene WFS1
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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00037405 - - - - - Germany - - - - - WFSL - WFS1 WFS1 1 1 Andreas Laner
00436608 2694995 Villafuerte-de la Cruz RA, et al., 2023. Submitted - M no Mexico Hispanic - - - None WFSL Reduced visual acuity HP:0007663, Nyctalopia HP:0000662, Peripheral visual field loss HP:0007994, Retinitis pigmentosa HP:0000510, Moderate sensorineural hearing impairment HP:0008504, Optic atrophy HP:0000648 WFS1 WFS1 1 1 Rocio Villafuerte-de la Cruz
00464549 - - - M no Israel Ashkenazi Jewish - - - - WFSL - - WFS1 1 1 Tamar Ben-Yosef
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