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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