Human Phenotype Ontology 
Grandparent Node:
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Fibroma (HP:0010614)help
Grandparent Node:
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Neoplasm of the peripheral nervous system (HP:0100007)help
Grandparent Node:
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Neoplasm of the skin (HP:0008069)help
Parent Node:
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Abnormal intestine morphology (HP:0002242)help
Parent Node:
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Neoplasm of the gastrointestinal tract (HP:0007378)help
Parent Node:
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Neurofibromas (HP:0001067)help
..Starting node
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Multiple intestinal neurofibromatosis (HP:0005220)help
Term ID: 5220
Name: Multiple intestinal neurofibromatosis
Synonym:
Definition:
Comments:
Reference: HP:0005220
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAtypical neurofibromatosis (HP:0007524) help
..expandOccasional neurofibromas (HP:0009595) help
..expandPalmar neurofibromas (HP:0007576) help
..expandParaspinal neurofibromas (HP:0006751) help
..expandPlexiform neurofibroma (HP:0009732) help
..expandSpinal neurofibromas (HP:0009735) help
..expandSubcutaneous neurofibromas (HP:0100698) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005220HP:0005220Multiple intestinal neurofibromatosis0 CL E G H


Genes (0) :

Diseases (0) :
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.