Disease #06848 (MRXS33 (Mental retardation, X-linked, syndromic 33), OMIM:300966)
Official abbreviation |
MRXS33 |
Name |
Mental retardation, X-linked, syndromic 33 |
OMIM ID |
300966 |
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 |
TAF1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|