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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