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Online Mendelian Inheritance in Man
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/OMIM/610199
http://purl.bioontology.org/ontology/OMIM/610199
|
|---|---|
| Preferred Name | DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM |
| Synonyms |
NDH SYNDROME
NDH
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
NDH SYNDROME
NDH
|
|---|---|
| prefLabel | DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM
|
| Gene Symbol |
GLIS3
NDH
ZNF515
|
| Scope Statement | Caused by mutation in the GLIS family zinc finger protein-3 (GLIS3, 610192.0001) [MOLECULAR BASIS]
Variable phenotype [MISCELLANEOUS]
|
| type | |
| Has manifestation |
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|
| tui | T047
|
| Gene Locus | 9p24.3-p23
|
| MIMTYPEMEANING | Phenotype description, molecular basis known.
|
| notation | 610199
|
| Semantic type UMLS property | |
| Has inheritance type | |
| cui | C1857775
|
| OMIM Entry Type | 3
|
| OMIM MimType Value | pound
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |