Human Phenotype Ontology 
Grandparent Node:
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Gastrointestinal dysmotility (HP:0002579)help
Grandparent Node:
expand
Intestinal obstruction (HP:0005214)help
Parent Node:
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Ileus (HP:0002595)help
..Starting node
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Mechanical ileus (HP:0010676)help
Term ID: 10676
Name: Mechanical ileus
Synonym:
Definition:
Comments:
Reference: HP:0010676
Genes and Diseases:
 
       Child Nodes:
........expandMeconium ileus (HP:0004401) help

 Sister Nodes: 
..expandParalytic ileus (HP:0002590) 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:0010676HP:0010676Mechanical ileus0CEACAM3 CL E G H10841815ORPHA:586Cystic fibrosis
HP:0010676HP:0010676Mechanical ileus0CEACAM6 CL E G H46801818ORPHA:586Cystic fibrosis1
HP:0010676HP:0010676Mechanical ileus0CFTR CL E G H10801884ORPHA:586Cystic fibrosis1371
HP:0010676HP:0010676Mechanical ileus0CFTR CL E G H10801884OMIM:219700Cystic fibrosis1371
HP:0010676HP:0010676Mechanical ileus0CLCA4 CL E G H228022018ORPHA:586Cystic fibrosis
HP:0010676HP:0010676Mechanical ileus0DCTN4 CL E G H5116415518ORPHA:586Cystic fibrosis
HP:0010676HP:0010676Mechanical ileus0EDNRA CL E G H19093179ORPHA:586Cystic fibrosis3
HP:0010676HP:0010676Mechanical ileus0FCGR2A CL E G H22123616OMIM:219700Cystic fibrosis6
HP:0010676HP:0010676Mechanical ileus0GCLC CL E G H27294311ORPHA:586Cystic fibrosis2
HP:0010676HP:0010676Mechanical ileus0GSTM3 CL E G H29474635ORPHA:586Cystic fibrosis1
HP:0010676HP:0010676Mechanical ileus0GUCY2C CL E G H29844688OMIM:614665Meconium ileus12
HP:0010676HP:0010676Mechanical ileus0HFE CL E G H30774886ORPHA:586Cystic fibrosis38
HP:0010676HP:0010676Mechanical ileus0HMOX1 CL E G H31625013ORPHA:586Cystic fibrosis3
HP:0010676HP:0010676Mechanical ileus0KCNN4 CL E G H37836293ORPHA:586Cystic fibrosis3
HP:0010676HP:0010676Mechanical ileus0MIF CL E G H42827097ORPHA:586Cystic fibrosis1
HP:0010676HP:0010676Mechanical ileus0SERPINA1 CL E G H52658941ORPHA:586Cystic fibrosis131
HP:0010676HP:0010676Mechanical ileus0SLC11A1 CL E G H655610907ORPHA:586Cystic fibrosis2
HP:0010676HP:0010676Mechanical ileus0SLC26A9 CL E G H11501914469ORPHA:586Cystic fibrosis5
HP:0010676HP:0010676Mechanical ileus0SLC6A14 CL E G H1125411047ORPHA:586Cystic fibrosis
HP:0010676HP:0010676Mechanical ileus0SLC9A3 CL E G H655011073ORPHA:586Cystic fibrosis7
HP:0010676HP:0010676Mechanical ileus0STX1A CL E G H680411433ORPHA:586Cystic fibrosis
HP:0010676HP:0010676Mechanical ileus0TGFB1 CL E G H704011766OMIM:219700Cystic fibrosis13
HP:0010676HP:0010676Mechanical ileus0TGFB1 CL E G H704011766ORPHA:586Cystic fibrosis13
HP:0010676HP:0004401Meconium ileus1CEACAM3 CL E G H10841815ORPHA:586Cystic fibrosis
HP:0010676HP:0004401Meconium ileus1CEACAM6 CL E G H46801818ORPHA:586Cystic fibrosis1
HP:0010676HP:0004401Meconium ileus1CFTR CL E G H10801884OMIM:219700Cystic fibrosis.1371
HP:0010676HP:0004401Meconium ileus1CFTR CL E G H10801884ORPHA:586Cystic fibrosis1371
HP:0010676HP:0004401Meconium ileus1CLCA4 CL E G H228022018ORPHA:586Cystic fibrosis
HP:0010676HP:0004401Meconium ileus1DCTN4 CL E G H5116415518ORPHA:586Cystic fibrosis
HP:0010676HP:0004401Meconium ileus1EDNRA CL E G H19093179ORPHA:586Cystic fibrosis3
HP:0010676HP:0004401Meconium ileus1FCGR2A CL E G H22123616OMIM:219700Cystic fibrosis.6
HP:0010676HP:0004401Meconium ileus1GCLC CL E G H27294311ORPHA:586Cystic fibrosis2
HP:0010676HP:0004401Meconium ileus1GSTM3 CL E G H29474635ORPHA:586Cystic fibrosis1
HP:0010676HP:0004401Meconium ileus1GUCY2C CL E G H29844688OMIM:614665Meconium ileus.12
HP:0010676HP:0004401Meconium ileus1HFE CL E G H30774886ORPHA:586Cystic fibrosis38
HP:0010676HP:0004401Meconium ileus1HMOX1 CL E G H31625013ORPHA:586Cystic fibrosis3
HP:0010676HP:0004401Meconium ileus1KCNN4 CL E G H37836293ORPHA:586Cystic fibrosis3
HP:0010676HP:0004401Meconium ileus1MIF CL E G H42827097ORPHA:586Cystic fibrosis1
HP:0010676HP:0004401Meconium ileus1SERPINA1 CL E G H52658941ORPHA:586Cystic fibrosis131
HP:0010676HP:0004401Meconium ileus1SLC11A1 CL E G H655610907ORPHA:586Cystic fibrosis2
HP:0010676HP:0004401Meconium ileus1SLC26A9 CL E G H11501914469ORPHA:586Cystic fibrosis5
HP:0010676HP:0004401Meconium ileus1SLC6A14 CL E G H1125411047ORPHA:586Cystic fibrosis
HP:0010676HP:0004401Meconium ileus1SLC9A3 CL E G H655011073ORPHA:586Cystic fibrosis7
HP:0010676HP:0004401Meconium ileus1STX1A CL E G H680411433ORPHA:586Cystic fibrosis
HP:0010676HP:0004401Meconium ileus1TGFB1 CL E G H704011766ORPHA:586Cystic fibrosis13
HP:0010676HP:0004401Meconium ileus1TGFB1 CL E G H704011766OMIM:219700Cystic fibrosis.13


Genes (21) :CEACAM3 CEACAM6 CFTR CLCA4 DCTN4 EDNRA FCGR2A GCLC GSTM3 GUCY2C HFE HMOX1 KCNN4 MIF SERPINA1 SLC11A1 SLC26A9 SLC6A14 SLC9A3 STX1A TGFB1

Diseases (3) :ORPHA:586 OMIM:219700 OMIM:614665
 

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