Disease #00103 (MRLIAF (mental retardation, language impairment, autistic features (MRLIAF)), OMIM:613670)
| Official abbreviation |
MRLIAF |
| Name |
mental retardation, language impairment, autistic features (MRLIAF) |
| OMIM ID |
613670 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
FOXP1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-01-16 09:42:45 +01:00 (CET) |
| Date last edited |
N/A |
|
