Disease #01125 (MRX63 (mental retardation, X-linked, type 63 (MRX63)), OMIM:300387)
Official abbreviation |
MRX63 |
Name |
mental retardation, X-linked, type 63 (MRX63) |
OMIM ID |
300387 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ACSL4 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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