Disease #03000 (CAHTP (choreoathetosis, hypothyroidism, and neonatal respiratory distress (CAHTP)), OMIM:610978)
| Official abbreviation |
CAHTP |
| Name |
choreoathetosis, hypothyroidism, and neonatal respiratory distress (CAHTP) |
| OMIM ID |
610978 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
NKX2-1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-03-16 10:53:35 +01:00 (CET) |
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