Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Localized skin lesion (HP:0011355)

Parent Node:
Autoamputation of foot (HP:0001868)

Parent Node:
Skin ulcer (HP:0200042)

..Starting node
..obsolete Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet) (HP:0001862)

Term ID:

1862

Name:

obsolete Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet)

Synonym:

Definition:

Comments:

Reference:

HP:0001862

Genes and Diseases:

Child Nodes:

Sister Nodes:

Acral ulceration (HP:0006121)

obsolete Acral ulceration and osteomyelitis leading to autoamputation of digits (HP:0001226)

Penetrating foot ulcers (HP:0001026)

Pressure ulcer (HP:0012399)

Pyoderma gangrenosum (HP:0025452)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0001862	HP:0001862	obsolete Acral ulceration and osteomyelitis leading to autoamputation of the digits (feet)	0	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 December 15 2022 release.