Human Phenotype Ontology 
Grandparent Node:
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Feeding difficulties (HP:0011968)help
Parent Node:
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Feeding difficulties in infancy (HP:0008872)help
..Starting node
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Gastrojejunal tube feeding in infancy (HP:0030884)help
Term ID: 30884
Name: Gastrojejunal tube feeding in infancy
Synonym: Gastro-jejunal tube feeding in infancy
Definition: Feeding problem necessitating gastrojejunal tube feeding.
Comments:
Reference: HP:0030884
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandGastrostomy tube feeding in infancy (HP:0011471) help
..expandNasal regurgitation (HP:0011469) help
..expandNasogastric tube feeding in infancy (HP:0011470) help
..expandPoor suck (HP:0002033) 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:0030884HP:0030884Gastrojejunal tube feeding in infancy0B3GALT6 CL E G H12679217978OMIM:609465AL-GAZALI SYNDROME38
HP:0030884HP:0030884Gastrojejunal tube feeding in infancy0EN1 CL E G H20193342OMIM:619218ENDOVE SYNDROME, LIMB-BRAIN TYPE; ENDOVESLB1
HP:0030884HP:0030884Gastrojejunal tube feeding in infancy0TXN2 CL E G H2582817772ORPHA:478029Combined oxidative phosphorylation defect type 29HP:0040281 - Very frequent1


Genes (3) :B3GALT6 EN1 TXN2

Diseases (3) :OMIM:609465 OMIM:619218 ORPHA:478029
 

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