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 2nd metacarpal morphology (HP:0010010)

Grandparent Node:
Metacarpal synostosis (HP:0009701)

Parent Node:
Metacarpophalangeal synostosis (HP:0005880)

Parent Node:
Symphalangism affecting the proximal phalanx of the 2nd finger (HP:0009586)

Parent Node:
Synostosis involving the 2nd metacarpal (HP:0009705)

..Starting node
..Symphalangism of the proximal phalanx of the 2nd finger with the 2nd metacarpal (HP:0009598)

Term ID:

9598

Name:

Symphalangism of the proximal phalanx of the 2nd finger with the 2nd metacarpal

Synonym:

Fused innermost bone of index finger with 2nd long bone of hand

Definition:

Fusion of the proximal phalanx of the 2nd finger with the 2nd metacarpal.

Comments:

Reference:

HP:0009598

Genes and Diseases:

Child Nodes:

Sister Nodes:

Synostosis of second metacarpal-trapezoid (HP:0004293)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009598	HP:0009598	Symphalangism of the proximal phalanx of the 2nd finger with the 2nd 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.