Disease #05032 (MRX12;MRX35 (mental retardation, X-linked, type 12/35 (MRX12;MRX35)), OMIM:300957)
Official abbreviation |
MRX12;MRX35 |
Name |
mental retardation, X-linked, type 12/35 (MRX12;MRX35) |
OMIM ID |
300957 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
THOC2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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