Preferred Name

HYPERPROINSULINEMIA

ID

http://purl.bioontology.org/ontology/OMIM/616214

cui

C0342283

Gene Locus

11p15.5

Gene Symbol

MODY10

INS

PNDM4

IDDM2

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU048115

http://purl.bioontology.org/ontology/OMIM/MTHU000372

http://purl.bioontology.org/ontology/OMIM/MTHU069939

http://purl.bioontology.org/ontology/OMIM/MTHU002042

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

616214

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

HYPERPROINSULINEMIA

Scope Statement

Caused by mutation in the insulin gene (INS, 176730.0001) [MOLECULAR BASIS]

tui

T047

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0014535 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/MESH/C562776 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/C562776 Medical Subject Headings / 医学主题词表 LOOM
http://www.ebi.ac.uk/efo/EFO_0009650 Experimental Factor Ontology / 实验性因素本体 LOOM