Human Phenotype Ontology 
Grandparent Node:
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Gastrointestinal dysmotility (HP:0002579)help
Grandparent Node:
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Intestinal obstruction (HP:0005214)help
Parent Node:
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Ileus (HP:0002595)help
..Starting node
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Paralytic ileus (HP:0002590)help
Term ID: 2590
Name: Paralytic ileus
Synonym:
Definition:
Comments:
Reference: HP:0002590
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMechanical ileus (HP:0010676) 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:0002590HP:0002590Paralytic ileus0FAH CL E G H21843579OMIM:276700Tyrosinemia, type I.107
HP:0002590HP:0002590Paralytic ileus0HMBS CL E G H31454982OMIM:176000Porphyria, acute intermittent.81
HP:0002590HP:0002590Paralytic ileus0MTRFR CL E G H9157426784ORPHA:254930Combined oxidative phosphorylation defect type 7HP:0040283 - Occasional
HP:0002590HP:0002590Paralytic ileus0MTRFR CL E G H9157426784OMIM:613559Combined oxidative phosphorylation deficiency 7.


Genes (3) :FAH HMBS MTRFR

Diseases (4) :OMIM:276700 OMIM:176000 ORPHA:254930 OMIM:613559
 

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