loading...| Preferred Name | DIABETES MELLITUS, TRANSIENT NEONATAL, 3 | |
| Synonyms |
DIABETES MELLITUS, TYPE II, AUTOSOMAL DOMINANT TNDM3 |
|
| ID |
http://purl.bioontology.org/ontology/OMIM/610582 |
|
| altLabel |
DIABETES MELLITUS, TYPE II, AUTOSOMAL DOMINANT TNDM3 |
|
| cui |
C1864623 C0342277 |
|
| Gene Locus |
11p15.1 |
|
| Gene Symbol |
BIR PNDM2 MODY13 PHHI KCNJ11 TNDM3 HHF2 |
|
| Has manifestation |
http://purl.bioontology.org/ontology/OMIM/MTHU068799 http://purl.bioontology.org/ontology/OMIM/MTHU002042 http://purl.bioontology.org/ontology/OMIM/MTHU036798 http://purl.bioontology.org/ontology/OMIM/MTHU068800 |
|
| MIMTYPEMEANING |
Phenotype description, molecular basis known. |
|
| notation |
610582 |
|
| OMIM Entry Type |
3 |
|
| OMIM MimType Value |
pound |
|
| prefLabel |
DIABETES MELLITUS, TRANSIENT NEONATAL, 3 |
|
| Scope Statement |
Onset in neonatal period (in some patients) [MISCELLANEOUS] Responsive to oral sulfonylurea (in some patients) [MISCELLANEOUS] Onset in 3rd decade of life (in some patients) [MISCELLANEOUS] Caused by mutation in the potassium inwardly-rectifying channel, subfamily J, member-11 gene (KCNJ11, 600937.0002) [MOLECULAR BASIS] |
|
| tui |
T047 |