Disease #05422 (MRFACD (mental retardation, distinctive facial features with/without cardiac defects), OMIM:616789)
| Official abbreviation |
MRFACD |
| Name |
mental retardation, distinctive facial features with/without cardiac defects |
| OMIM ID |
616789 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
MED13L |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2018-05-04 13:48:09 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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