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:
Finger symphalangism (HP:0009700)

Grandparent Node:
Symphalangism affecting the phalanges of the hand (HP:0009773)

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

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

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

..Starting node
..Symphalangism of middle phalanx of 3rd finger (HP:0009435)

Term ID:

9435

Name:

Symphalangism of middle phalanx of 3rd finger

Synonym:

Fused middle bone of middle finger

Definition:

Fusion of the middle phalanx of the 3rd finger with another bone.

Comments:

Reference:

HP:0009435

Genes and Diseases:

Child Nodes:

........

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

........

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

Sister Nodes:

Symphalangism affecting the proximal phalanx of the 3rd finger (HP:0009455)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009435	HP:0009435	Symphalangism of middle phalanx of 3rd finger	0	CL E G H
HP:0009435	HP:0009482	Proximal/middle symphalangism of 3rd finger	1	CL E G H
HP:0009435	HP:0009426	Distal/middle symphalangism of 3rd finger	1	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.