Disease #00801 (MRT13 (mental retardation, autosomal recessive, type 13), OMIM:613192)
| Official abbreviation |
MRT13 |
| Name |
mental retardation, autosomal recessive, type 13 |
| OMIM ID |
613192 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
3 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
TRAPPC9 |
| Associated tissues |
- |
| Disease features |
hypoplastic supraorbital ridges; global developmental delay (HP:0001263); intellectual disability (HP:0001249); seizure (HP:0001250); hypotonia (HP:0001252); no short stature (-HP:0004322); obesity (HP:0001513); digital abnormalities (HP_0011297); tapering fingers, stereotypies, MRI changes (cerebral and cerebellar atrophy, thin corpus callosum, and multifocal supratentorial white matter abnormalities) |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-01-03 20:52:12 +01:00 (CET) |
Individuals
|