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 phalanges of the toes (HP:0010161)

Grandparent Node:
Broad phalanx (HP:0006009)

Grandparent Node:
obsolete Abnormal morphology of bones of the lower limbs (HP:0040066)

Parent Node:
Abnormality of the middle phalanges of the toes (HP:0010183)

Parent Node:
Broad phalanx of the toes (HP:0010174)

..Starting node
..Broad middle phalanges of the toes (HP:0010195)

Term ID:

10195

Name:

Broad middle phalanges of the toes

Synonym:

Broad middle bones of the toes

Definition:

Comments:

Reference:

HP:0010195

Genes and Diseases:

Child Nodes:

........

Broad middle phalanx of the 2nd toe (HP:0010405)

........

Broad middle phalanx of the 3rd toe (HP:0100425)

........

Broad middle phalanx of the 4th toe (HP:0100426)

........

Broad middle phalanx of the 5th toe (HP:0100427)

Sister Nodes:

Broad distal phalanx of the toes (HP:0010186)

Broad hallux phalanx (HP:0010059)

Broad phalanges of the 2nd toe (HP:0010348)

Broad phalanges of the 3rd toe (HP:0010360)

Broad phalanges of the 4th toe (HP:0010372)

Broad phalanges of the 5th toe (HP:0010384)

Broad proximal phalanx of toe (HP:0010204)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010195	HP:0010195	Broad middle phalanges of the toes	0	CL E G H
HP:0010195	HP:0100427	Broad middle phalanx of the 5th toe	1	CL E G H
HP:0010195	HP:0100426	Broad middle phalanx of the 4th toe	1	CL E G H
HP:0010195	HP:0100425	Broad middle phalanx of the 3rd toe	1	CL E G H
HP:0010195	HP:0010405	Broad middle phalanx of the 2nd toe	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.