Disease #06849 (MRXS99F (Mental retardation, X-linked 99, syndromic, female-restricted), OMIM:300968)
Official abbreviation |
MRXS99F |
Name |
Mental retardation, X-linked 99, syndromic, female-restricted |
OMIM ID |
300968 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked dominant |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
USP9X |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|
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