Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Abnormality of the phalanges of the 3rd toe (HP:0010330)

Grandparent Node:
Osteolytic defects of the phalanges of the toes (HP:0010177)

Parent Node:
Osteolytic defects of the phalanges of the 3rd toe (HP:0010363)

..Starting node
..Osteolytic defects of the middle phalanx of the 3rd toe (HP:0100452)

Term ID:

100452

Name:

Osteolytic defects of the middle phalanx of the 3rd toe

Synonym:

Definition:

Comments:

Reference:

HP:0100452

Genes and Diseases:

Child Nodes:

Sister Nodes:

Osteolytic defects of the distal phalanx of the 3rd toe (HP:0100458)

Osteolytic defects of the proximal phalanx of the 3rd toe (HP:0100455)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100452	HP:0100452	Osteolytic defects of the middle phalanx of the 3rd toe	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.