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 skeletal maturation (HP:0000927)

Parent Node:
Accelerated skeletal maturation (HP:0005616)

Parent Node:
Dysharmonic bone age (HP:0200000)

..Starting node
..Dysharmonic accelerated bone age (HP:0200001)

Term ID:

200001

Name:

Dysharmonic accelerated bone age

Synonym:

Definition:

A type of dysharmonic skeletal maturation in which there is an acceleration in skeletal maturation whose degree differs markedly in different bones.

Comments:

Reference:

HP:0200001

Genes and Diseases:

Child Nodes:

Sister Nodes:

Dysharmonic delayed bone age (HP:0005832)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0200001	HP:0200001	Dysharmonic accelerated bone age	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.