Human Phenotype Ontology 
Grandparent Node:
expandMorphological abnormality of the gastrointestinal tract (HP:0012718)help
Parent Node:
expandAbnormal stomach morphology (HP:0002577)help
..Starting node
..expandAbsence of intrinsic factor (HP:0005219)help
Term ID: 5219
Name: Absence of intrinsic factor
Synonym: Intrinsic factor absent from gastric juice
Definition: Absence of gastric intrinsic factor, which is normally produced by the parietal cells of the stomach, and is required for the absorption of vitamin B12.
Comments:
Reference: HP:0005219
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal gastric mucosa morphology (HP:0004295) help
..expandAbnormality of the pylorus (HP:0004400) help
..expandGastric diverticulum (HP:0100808) help
..expandGastric duplication (HP:0011139) help
..expandGastric hypertrophy (HP:0005207) help
..expandGastric varix (HP:0030169) help
..expandGastroesophageal reflux (HP:0002020) help
..expandGastroparesis (HP:0002578) help
..expandHiatus hernia (HP:0002036) help
..expandMalposition of the stomach (HP:0100802) help
..expandMicrogastria (HP:0100841) help
..expandNeoplasm of the stomach (HP:0006753) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005219HP:0005219Absence of intrinsic factor0CBLIF CL E G H26944268OMIM:261000Intrinsic factor deficiency.


Genes (1) :CBLIF

Diseases (1) :OMIM:261000
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.