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:
Abnormal 3rd metacarpal morphology (HP:0010011)

Grandparent Node:
Metacarpal synostosis (HP:0009701)

Parent Node:
Metacarpophalangeal synostosis (HP:0005880)

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

Parent Node:
Synostosis involving the 3rd metacarpal (HP:0009706)

..Starting node
..Symphalangism of the proximal phalanx of the 3rd finger with the 3rd metacarpal (HP:0009483)

Term ID:

9483

Name:

Symphalangism of the proximal phalanx of the 3rd finger with the 3rd metacarpal

Synonym:

Fused innermost bones of middle finger with middle long bone of hand

Definition:

Fusion of the proximal phalanx of the 3rd finger with the 3rd metacarpal.

Comments:

Reference:

HP:0009483

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009483	HP:0009483	Symphalangism of the proximal phalanx of the 3rd finger with the 3rd metacarpal	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.