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 1
Phenotype entries for this disease 1
Associated with 1 gene WFS1
Associated tissues -
Disease features -
Remarks -


Individuals

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00037405 - - - - - Germany - - 0 - - WFSL - WFS1 WFS1 1 1 Andreas Laner
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