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:
Abnormal 3rd finger phalanx morphology (HP:0009316)

Grandparent Node:
Broad phalanges of the hand (HP:0009768)

Parent Node:
Abnormality of the middle phalanx of the 3rd finger (HP:0004172)

Parent Node:
Broad middle phalanx of finger (HP:0009844)

Parent Node:
Broad phalanges of the 3rd finger (HP:0009440)

..Starting node
..Broad middle phalanx of the 3rd finger (HP:0009430)

Term ID:

9430

Name:

Broad middle phalanx of the 3rd finger

Synonym:

Broad middle bone of middle finger; Wide/broad middle phalanx of middle-finger

Definition:

Increased width of the middle phalanx of the 3rd finger.

Comments:

Reference:

HP:0009430

Genes and Diseases:

Child Nodes:

Sister Nodes:

Broad distal phalanx of the 3rd finger (HP:0009422)

Broad proximal phalanx of the 3rd finger (HP:0009450)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009430	HP:0009430	Broad middle phalanx of the 3rd 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.