Disease #03982 (MRT38 (mental retardation, autosomal recessive, type 38 (MRT38)), OMIM:615516)
| Official abbreviation |
MRT38 |
| Name |
mental retardation, autosomal recessive, type 38 (MRT38) |
| OMIM ID |
615516 |
| 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 |
HERC2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-05-17 13:27:38 +02:00 (CEST) |
Individuals
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