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 toes (HP:0010160)

Grandparent Node:
Small epiphyses (HP:0010585)

Parent Node:
Abnormality of the epiphyses of the 3rd toe (HP:0010329)

Parent Node:
Small epiphyses of the toes (HP:0010170)

..Starting node
..Small epiphyses of the 3rd toe (HP:0100063)

Term ID:

100063

Name:

Small epiphyses of the 3rd toe

Synonym:

Small end part of the 3rd toe bone

Definition:

Comments:

Reference:

HP:0100063

Genes and Diseases:

Child Nodes:

........

Small epiphysis of the distal phalanx of the 3rd toe (HP:0100143)

........

Small epiphysis of the middle phalanx of the 3rd toe (HP:0100154)

........

Small epiphysis of the proximal phalanx of the 3rd toe (HP:0100165)

Sister Nodes:

Small epiphyses of the 2nd toe (HP:0100052)

Small epiphyses of the 4th toe (HP:0100074)

Small epiphyses of the 5th toe (HP:0100085)

Small epiphyses of the hallux (HP:0010121)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100063	HP:0100063	Small epiphyses of the 3rd toe	0	CL E G H
HP:0100063	HP:0100165	Small epiphysis of the proximal phalanx of the 3rd toe	1	CL E G H
HP:0100063	HP:0100154	Small epiphysis of the middle phalanx of the 3rd toe	1	CL E G H
HP:0100063	HP:0100143	Small epiphysis of the distal phalanx of the 3rd toe	1	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.