Disease #02207 (MRX99 (mental retardation, X-linked, type 99 (MRX99)), OMIM:300919)
Official abbreviation |
MRX99 |
Name |
mental retardation, X-linked, type 99 (MRX99) |
OMIM ID |
300919 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
USP9X |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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