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 |
Autosomal dominant |
Individuals reported having this disease |
4 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
FOXP1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-01-16 09:42:45 +01:00 (CET) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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