Disease #06590 (HIDEA (Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities), OMIM:618493)
| Official abbreviation |
HIDEA |
| Name |
Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities |
| OMIM ID |
618493 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
6 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
P4HTM |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
|