Disease #04666 (MRT48 (mental retardation, autosomal recessive, type 48 (MRT-48)), OMIM:616269)
| Official abbreviation |
MRT48 |
| Name |
mental retardation, autosomal recessive, type 48 (MRT-48) |
| OMIM ID |
616269 |
| 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 |
SLC6A17 |
| 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
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