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 epiphyses of the proximal phalanges of the hand (HP:0010245)

Grandparent Node:
Cone-shaped epiphyses of the phalanges of the hand (HP:0010230)

Parent Node:
Abnormality of the epiphysis of the proximal phalanx of the 2nd finger (HP:0009501)

Parent Node:
Cone-shaped epiphyses of the 2nd finger (HP:0009490)

Parent Node:
Cone-shaped epiphyses of the proximal phalanges of the hand (HP:0010270)

..Starting node
..Cone-shaped epiphysis of the proximal phalanx of the 2nd finger (HP:0009526)

Term ID:

9526

Name:

Cone-shaped epiphysis of the proximal phalanx of the 2nd finger

Synonym:

Cone-shaped end part of innermost long bone of index finger; Cone-shaped epiphysis of proximal index finger phalanx

Definition:

Comments:

Reference:

HP:0009526

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cone-shaped epiphysis of the 1st metacarpal (HP:0010017)

Cone-shaped epiphysis of the proximal phalanx of the 3rd finger (HP:0009348)

Cone-shaped epiphysis of the proximal phalanx of the 4th finger (HP:0009263)

Cone-shaped epiphysis of the proximal phalanx of the 5th finger (HP:0009155)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009526	HP:0009526	Cone-shaped epiphysis of the proximal phalanx of the 2nd finger	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.