Maturity-onset diabetes of the young, type 13

Preferred Label : Maturity-onset diabetes of the young, type 13;

Symbol : MODY13;

CISMeF acronym : MODY13;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Mody, type 13;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the potassium inwardly-rectifying channel, subfamily J, member 11 gene (KCNJ11, 600937.0012);

Prefixed ID : #616329;

Détails

Origin ID

616329;

UMLS CUI

C4225365;

CISMeF manual mappings
- maturity-onset diabetes of the young type 13 [DO Concept]
DO Cross reference
- maturity-onset diabetes of the young type 13 [DO Concept]
Genes related to phenotype
- Potassium channel, inwardly rectifying, subfamily j, member 11 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Maternal diabetes [HPO term]
- Maturity-onset diabetes of the young [HPO term]
Not associated HPO term(s)
- Abnormality of body mass index [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 13 [DO Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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