Disease association ontology term - MONDO:0015967 - monogenic diabetes

Term summary

ID: MONDO:0015967
Name: monogenic diabetes
Ontology or CV name: Disease association
Definition: Diabetes mellitus that is caused by mutations in a single gene.

Parents

is_a diabetes mellitus
is_a inborn errors of metabolism

Annotation

Disease association

MONDO:0015967 - monogenic diabetes

References:

Genes:

MONDO:0018911 - maturity-onset diabetes of the young

References:

PB_REF:0000003

Genes:

hxk1 (SPAC24H6.04)

MONDO:0014674 - maturity-onset diabetes of the young type 14

References:

PB_REF:0000006

Genes:

ltc2 (SPAC19A8.02)

MONDO:0007453 - maturity-onset diabetes of the young type 2

References:

PB_REF:0000006

Genes:

MONDO:0016391 - neonatal diabetes mellitus

References:

PB_REF:0000003

Genes:

MONDO:0100165 - permanent neonatal diabetes mellitus 1

References:

PB_REF:0000006

Genes: