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 phalanx (HP:0009602)

Parent Node:
Abnormality of the proximal phalanx of the thumb (HP:0009618)

Parent Node:
Triangular shaped middle phalanges of the hand (HP:0009850)

Parent Node:
Triangular shaped proximal phalanges of the hand (HP:0009858)

Parent Node:
Triangular shaped thumb phalanx (HP:0009657)

..Starting node
..Triangular shaped proximal phalanx of the thumb (HP:0009636)

Term ID:

9636

Name:

Triangular shaped proximal phalanx of the thumb

Synonym:

Triangular innermost thumb bone; Triangular proximal thumb phalanx

Definition:

Triangular shaped proximal phalanx of the thumb.

Comments:

Reference:

HP:0009636

Genes and Diseases:

Child Nodes:

Sister Nodes:

Triangular shaped distal phalanx of the thumb (HP:0009648)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009636	HP:0009636	Triangular shaped 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.