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:
Abnormality of the epiphyses of the hallux (HP:0010056)

Grandparent Node:
Absent epiphyses of the toes (HP:0010162)

Parent Node:
Abnormality of the epiphysis of the proximal phalanx of the hallux (HP:0010126)

Parent Node:
Absent hallux epiphysis (HP:0010113)

..Starting node
..Absent epiphysis of the proximal phalanx of the hallux (HP:0010127)

Term ID:

10127

Name:

Absent epiphysis of the proximal phalanx of the hallux

Synonym:

Absent end part of the innermost bone of the big toe

Definition:

Failure to form (agenesis) of the epiphysis of the proximal phalanx of the hallux.

Comments:

Reference:

HP:0010127

Genes and Diseases:

Child Nodes:

Sister Nodes:

Absent epiphysis of the distal phalanx of the hallux (HP:0010138)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010127	HP:0010127	Absent epiphysis of the proximal phalanx of the hallux	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.