Disease #01073 (MRXHF1 (mental retardation-hypotonic facies syndrome, X-linked), OMIM:309580)
Official abbreviation |
MRXHF1 |
Name |
mental retardation-hypotonic facies syndrome, X-linked |
OMIM ID |
309580 |
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 |
ATRX |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|