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 epiphysis morphology (HP:0005930)

Parent Node:
Abnormal metacarpal epiphysis morphology (HP:0005913)

Parent Node:
Increased bone mineral density (HP:0011001)

Parent Node:
Ivory epiphyses (HP:0010583)

..Starting node
..Ivory epiphyses of the metacarpals (HP:0009191)

Term ID:

9191

Name:

Ivory epiphyses of the metacarpals

Synonym:

Increased bone density of end part of the long bone of hands

Definition:

Sclerosis of the epiphyses of the metacarpals, leading to an increased degree of radiopacity (white or ivory appearance) in X-rays.

Comments:

Reference:

HP:0009191

Genes and Diseases:

Child Nodes:

........

Ivory epiphysis of the 1st metacarpal (HP:0010021)

Sister Nodes:

Ivory epiphyses of the phalanges of the hand (HP:0010234)

Ivory epiphyses of the toes (HP:0010168)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009191	HP:0009191	Ivory epiphyses of the metacarpals	0	CL E G H
HP:0009191	HP:0010021	Ivory epiphysis of the 1st metacarpal	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.