Disease #01117 (mental retardation, X-linked syndromic, Fried type, OMIM:300630)
Official abbreviation |
- |
Name |
mental retardation, X-linked syndromic, Fried type |
OMIM ID |
300630 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
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Associated with 1 gene |
AP1S2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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