Disease #00345 (CFHD (deficiency, complement factor H (CFHD)), OMIM:609814)

Official abbreviation CFHD
Name deficiency, complement factor H (CFHD)
OMIM ID 609814
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CFH
Associated tissues -
Disease features -
Remarks -

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