(Q2467739)

Statements

instance of

rare disease

0 references

class of disease

0 references

subclass of

autosomal recessive disease

1 reference

stated in

Disease Ontology

retrieved

30 November 2020

Disease Ontology ID

DOID:0050470

diabetes

0 references

syndrome

1 reference

stated in

Disease Ontology

retrieved

30 November 2020

Disease Ontology ID

DOID:0050470

image

PBB Protein INSR image.jpg
500 × 500; 35 KB

1 reference

imported from Wikimedia project

Dutch Wikipedia

health specialty

endocrinology

0 references

rheumatology

0 references

medical genetics

0 references

genetic association

INSR

2 references

stated in

Leprechaunism and homozygous nonsense mutation in the insulin receptor gene.

stated in

Open Targets Platform

retrieved

24 August 2023

reference URL

https://platform.opentargets.org/evidence/ENSG00000171105/Orphanet_508

based on heuristic

inferred from an Open Targets association score over 0.7

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C84676

1 reference

stated in

Disease Ontology

retrieved

28 August 2019

Disease Ontology ID

DOID:0050470

C131000

1 reference

stated in

Disease Ontology

retrieved

28 August 2019

Disease Ontology ID

DOID:0050470

exact match

http://purl.obolibrary.org/obo/DOID_0050470

1 reference

stated in

Disease Ontology

retrieved

30 November 2020

Disease Ontology ID

DOID:0050470

http://identifiers.org/doid/DOID:0050470

1 reference

stated in

Identifiers.org

reference URL

https://registry.identifiers.org/registry/doid

Identifiers