Disease #03730 (CFHR5 deficiency, OMIM:614809)
Official abbreviation |
- |
Name |
CFHR5 deficiency |
OMIM ID |
614809 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
CFHR5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|
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