Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the digestive system (HP:0025031)help
Parent Node:
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Abnormality of digestive system physiology (HP:0025032)help
..Starting node
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Dependency on intravenous nutrition (HP:0025156)help
Term ID: 25156
Name: Dependency on intravenous nutrition
Synonym: Dependency on IV nutrition
Definition: Inability to be weaned from intravenous (parenteral) nutrition, as judged by the hydration status (urine output, blood urea nitrogen, creatinine, urine sodium concentration), ability to maintain weight, stool output, and serum electrolyte status.
Comments:
Reference: HP:0025156
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbdominal symptom (HP:0011458) help
..expandAbnormal large intestine physiology (HP:0012700) help
..expandAbnormality of hepatobiliary system physiology (HP:0025155) help
..expandFunctional abnormality of the gastrointestinal tract (HP:0012719) 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:0025156HP:0025156Dependency on intravenous nutrition0FOXP3 CL E G H509436106ORPHA:37042Immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndromeHP:0040284 - Very rare32
HP:0025156HP:0025156Dependency on intravenous nutrition0SKIC2 CL E G H649910898ORPHA:84064Syndromic diarrheaHP:0040282 - Frequent
HP:0025156HP:0025156Dependency on intravenous nutrition0SKIC3 CL E G H965223639ORPHA:84064Syndromic diarrheaHP:0040282 - Frequent


Genes (3) :FOXP3 SKIC2 SKIC3

Diseases (2) :ORPHA:37042 ORPHA:84064
 

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