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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