congenital intrinsic factor deficiency

Summary

DOID:0050734 - congenital intrinsic factor deficiency

Disease Ontology Definition:A vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption.

Synonyms: hereditary intrinsic factor deficiency

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: cblif

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0009852 - hereditary intrinsic factor deficiency

MONDO:0009852 - hereditary intrinsic factor deficiency

MIM:

MIM:261000 - INTRINSIC FACTOR DEFICIENCY; IFD

MIM:261000 - INTRINSIC FACTOR DEFICIENCY; IFD

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): physical disorder (is_a), vitamin B12 deficiency (is_a)