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 morphology of phalanx of the 2nd toe (HP:0010324)

Grandparent Node:
Triangular shaped phalanges of the toes (HP:0010180)

Parent Node:
Abnormality of the middle phalanx of the 2nd toe (HP:0010357)

Parent Node:
Triangular shaped phalanges of the 2nd toe (HP:0010354)

..Starting node
..Triangular shaped middle phalanx of the 2nd toe (HP:0010411)

Term ID:

10411

Name:

Triangular shaped middle phalanx of the 2nd toe

Synonym:

Triangular shaped middle bone of 2nd toe

Definition:

Comments:

Reference:

HP:0010411

Genes and Diseases:

Child Nodes:

Sister Nodes:

Triangular shaped distal phalanx of the 2nd toe (HP:0010420)

Triangular shaped proximal phalanx of the 2nd toe (HP:0010402)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010411	HP:0010411	Triangular shaped middle phalanx of the 2nd toe	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.