Disease #05466 (EHLMRS (epilepsy, hearing loss, and mental retardation syndrome (EHLMRS)), OMIM:616577)
Official abbreviation |
EHLMRS |
Name |
epilepsy, hearing loss, and mental retardation syndrome (EHLMRS) |
OMIM ID |
616577 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
SPATA5 |
Associated tissues |
- |
Disease features |
autosomal recessive |
Remarks |
- |
Date created |
2018-08-17 11:43:30 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|