Disease #00167 (FANCM (Fanconi anemia, complementation group M), OMIM:614087)
| Official abbreviation |
FANCM |
| Name |
Fanconi anemia, complementation group M |
| OMIM ID |
614087 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-07-21 20:43:53 +02:00 (CEST) |
| Date last edited |
2025-02-24 14:29:25 +01:00 (CET) |
Individuals
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