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:
Pseudoepiphyses of the phalanges of the hand (HP:0010235)

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

Parent Node:
Pseudoepiphyses of the middle phalanges of the hand (HP:0010264)

Parent Node:
Pseudoepiphysis of the thumb (HP:0009693)

..Starting node
..Pseudoepiphysis of the proximal phalanx of the thumb (HP:0009671)

Term ID:

9671

Name:

Pseudoepiphysis of the proximal phalanx of the thumb

Synonym:

Definition:

A pseudoepiphysis (which is a secondary ossification center distinct from the normal epiphysis) of the proximal phalanx of the thumb.

Comments:

Reference:

HP:0009671

Genes and Diseases:

Child Nodes:

Sister Nodes:

Pseudoepiphysis of the distal phalanx of the thumb (HP:0009682)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009671	HP:0009671	Pseudoepiphysis 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.