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 5th finger (HP:0004219)

Grandparent Node:
Triangular shaped middle phalanges of the hand (HP:0009850)

Grandparent Node:
Triangular shaped phalanges of the 5th finger (HP:0009378)

Parent Node:
Triangular shaped middle phalanx of the 5th finger (HP:0009182)

..Starting node
..Rhomboid or triangular shaped 5th finger middle phalanx (HP:0005910)

Term ID:

5910

Name:

Rhomboid or triangular shaped 5th finger middle phalanx

Synonym:

Rhomboid or triangular shaped fifth finger middle phalanx

Definition:

Rhomboid or triangular shaped 5th (little) finger middle phalanx.

Comments:

Reference:

HP:0005910

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:0005910	HP:0005910	Rhomboid or triangular shaped 5th finger middle phalanx	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.