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 thumb epiphysis (HP:0009599)

Grandparent Node:
Small epiphyses of the phalanges of the hand (HP:0010236)

Parent Node:
Abnormality of the epiphysis of the proximal phalanx of the thumb (HP:0009663)

Parent Node:
Small epiphyses of the middle phalanges of the hand (HP:0010265)

Parent Node:
Small thumb epiphysis (HP:0009694)

..Starting node
..Small epiphysis of the proximal phalanx of the thumb (HP:0009672)

Term ID:

9672

Name:

Small epiphysis of the proximal phalanx of the thumb

Synonym:

Small end part of thumb innermost long bone

Definition:

Abnormally small size of the epiphysis located at the proximal end of the proximal phalanx of the thumb with respect to age-dependent norms.

Comments:

Reference:

HP:0009672

Genes and Diseases:

Child Nodes:

Sister Nodes:

Small epiphysis of the distal phalanx of the thumb (HP:0009683)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009672	HP:0009672	Small epiphysis of the proximal phalanx of the thumb	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.