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

Grandparent Node:
Symphalangism of middle phalanx of finger (HP:0009849)

Grandparent Node:
Symphalangism of the 3rd finger (HP:0009445)

Parent Node:
Abnormality of the distal phalanx of the 3rd finger (HP:0009357)

Parent Node:
Distal symphalangism of hands (HP:0001204)

Parent Node:
Symphalangism of middle phalanx of 3rd finger (HP:0009435)

..Starting node
..Distal/middle symphalangism of 3rd finger (HP:0009426)

Term ID:

9426

Name:

Distal/middle symphalangism of 3rd finger

Synonym:

Fused outermost and middle bones of middle finger; Symphalangism of the distal and middle phalanges of the 3rd finger

Definition:

Fusion of the terminal/distal and middle phalanges of the 3rd finger.

Comments:

Reference:

HP:0009426

Genes and Diseases:

Child Nodes:

Sister Nodes:

Proximal/middle symphalangism of 3rd finger (HP:0009482)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009426	HP:0009426	Distal/middle symphalangism of 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.