Disease #07036 (IDDHISD (intellectual developmental disorder with hypotonia, impaired speech, dysmorphic facies), OMIM:619556)
| Official abbreviation |
IDDHISD |
| Name |
intellectual developmental disorder with hypotonia, impaired speech, dysmorphic facies |
| OMIM ID |
619556 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TNPO2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-10-23 16:49:47 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|