Disease #05182 (IHPRF2 (hypotonia, infantile, with psychomotor retardation and characteristic facies, type 2 (IHPRF-2)), OMIM:616801)
| Official abbreviation |
IHPRF2 |
| Name |
hypotonia, infantile, with psychomotor retardation and characteristic facies, type 2 (IHPRF-2) |
| OMIM ID |
616801 |
| 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 |
UNC80 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2016-09-13 16:07:19 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|