congenital intrinsic factor deficiency
vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption
Press Enter · cited answer in seconds
0 sources
congenital intrinsic factor deficiency
Summary
congenital intrinsic factor deficiency is a class of disease[1].
Key Facts
- congenital intrinsic factor deficiency's instance of is recorded as class of disease[2].
- congenital intrinsic factor deficiency's subclass of is recorded as vitamin B12 deficiency[3].
- congenital intrinsic factor deficiency's subclass of is recorded as inborn disorder of cobalamin metabolism and transport[4].
- congenital intrinsic factor deficiency's subclass of is recorded as vitamin B12 deficiency anemia[5].
- congenital intrinsic factor deficiency's subclass of is recorded as congenital disorder[6].
- congenital intrinsic factor deficiency's MeSH descriptor ID is recorded as C563242[7].
- congenital intrinsic factor deficiency's OMIM ID is recorded as 261000[8].
- congenital intrinsic factor deficiency's Disease Ontology ID is recorded as DOID:0050734[9].
- congenital intrinsic factor deficiency's Orphanet ID is recorded as 332[10].
- congenital intrinsic factor deficiency's ICD-9-CM is recorded as 281.3[11].
- congenital intrinsic factor deficiency's genetic association is recorded as CBLIF[12].
- congenital intrinsic factor deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050734[13].
- congenital intrinsic factor deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0050734[14].
- congenital intrinsic factor deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_332[15].
- congenital intrinsic factor deficiency's UMLS CUI is recorded as C1394891[16].
- congenital intrinsic factor deficiency's UMLS CUI is recorded as C0340957[17].
- congenital intrinsic factor deficiency's ICD-10-CM is recorded as D51.0[18].
- congenital intrinsic factor deficiency's GARD rare disease ID is recorded as 3024[19].
- congenital intrinsic factor deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
- congenital intrinsic factor deficiency's Mondo ID is recorded as MONDO_0009852[21].
- congenital intrinsic factor deficiency's has phenotype is recorded as vitamin B12 deficiency[22].
- congenital intrinsic factor deficiency's UniProt disease ID is recorded as DI-01720[23].