Human Phenotype Ontology 
Grandparent Node:
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Abnormality of limbs (HP:0040064)help
Parent Node:
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Abnormal foot morphology (HP:0001760)help
Parent Node:
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Autoamputation (HP:0001218)help
..Starting node
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Autoamputation of foot (HP:0001868)help
Term ID: 1868
Name: Autoamputation of foot
Synonym:
Definition: Spontaneous detachment of a foot from the body.
Comments:
Reference: HP:0001868
Genes and Diseases:
 
       Child Nodes:
........expandAcral ulceration and osteomyelitis leading to autoamputation of the digits (feet) (HP:0001862) help

 Sister Nodes: 
..expandAutoamputation of digits (HP:0007460) 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:0001868HP:0001868Autoamputation of foot0RAB7A CL E G H78799788OMIM:600882Charcot-Marie-Tooth disease, axonal, type 2B.50
HP:0001868HP:0001868Autoamputation of foot0SPTLC1 CL E G H1055811277OMIM:162400Neuropathy, hereditary sensory and autonomic, type IA.54


Genes (2) :RAB7A SPTLC1

Diseases (2) :OMIM:600882 OMIM:162400
 

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