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:
Osteolytic defects of the phalanges of the toes (HP:0010177)

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

Parent Node:
Osteolytic defects of the phalanges of the 2nd toe (HP:0010351)

..Starting node
..Osteolytic defects of the middle phalanx of the 2nd toe (HP:0010408)

Term ID:

10408

Name:

Osteolytic defects of the middle phalanx of the 2nd toe

Synonym:

Definition:

Comments:

Reference:

HP:0010408

Genes and Diseases:

Child Nodes:

Sister Nodes:

Osteolytic defects of the distal phalanx of the 2nd toe (HP:0010417)

Osteolytic defects of the proximal phalanx of the 2nd toe (HP:0010399)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010408	HP:0010408	Osteolytic defects of the 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.