Disease #02914 (NDH (diabetes mellitus, neonatal, with congenital hypothyroidism (NDH)), OMIM:610199)
| Official abbreviation |
NDH |
| Name |
diabetes mellitus, neonatal, with congenital hypothyroidism (NDH) |
| OMIM ID |
610199 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
GLIS3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-03-16 10:54:12 +01:00 (CET) |
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