Maturity-onset diabetes of the young, type 10

Preferred Label : Maturity-onset diabetes of the young, type 10;

Symbol : MODY10;

CISMeF acronym : MODY10;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the insulin gene (INS, 176730.0014);

Prefixed ID : #613370;

Details

Origin ID

613370;

UMLS CUI

C3150617;

Automatic exact mappings (from CISMeF team)
- MODY [ORDO Disease]
Currated CISMeF NLP mapping
- Maturity-onset diabetes of the young, type 10 (disorder) [SNOMED CT concept]
- maturity-onset diabetes of the young type 10 [DO Concept]
DO Cross reference
- maturity-onset diabetes of the young type 10 [DO Concept]
Genes related to phenotype
- Insulin [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Diabetes mellitus [HPO term]
- Diabetic ketoacidosis [HPO term]
- Hyperglycemia [HPO term]
- Intrauterine growth retardation [HPO term]
- Maturity-onset diabetes of the young [HPO term]
ORDO concept(s)
- MODY [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Maturity-onset diabetes of the young, type 10 (disorder) [SNOMED CT concept]
- maturity-onset diabetes of the young type 10 [DO Concept]

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