Disease #00822 (MRX1 (mental retardation, X-linked, type 1), OMIM:309530)
Official abbreviation |
MRX1 |
Name |
mental retardation, X-linked, type 1 |
OMIM ID |
309530 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
IQSEC2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2022-11-25 16:08:47 +01:00 (CET) |
Individuals
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