Disease #04572 (MRXS13 (mental retardation, X-linked, syndromic, type 13 (MRX13)), OMIM:300055)
Official abbreviation |
MRXS13 |
Name |
mental retardation, X-linked, syndromic, type 13 (MRX13) |
OMIM ID |
300055 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
MECP2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-09-23 10:25:23 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|