Disease #00345 (CFHD (complement factor H deficiency (CFHD)), OMIM:609814)
| Official abbreviation |
CFHD |
| Name |
complement factor H deficiency (CFHD) |
| OMIM ID |
609814 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CFH |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-03-13 09:50:57 +01:00 (CET) |
| Date last edited |
N/A |
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