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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