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:
Abnormally ossified vertebrae (HP:0100569)

Parent Node:
Absent or minimally ossified vertebral bodies (HP:0004599)

..Starting node
..Absent ossification of cervical vertebral bodies (HP:0005885)

Term ID:

5885

Name:

Absent ossification of cervical vertebral bodies

Synonym:

Definition:

A lack of bone mineralization of one or more body of cervical vertebra.

Comments:

Reference:

HP:0005885

Genes and Diseases:

Child Nodes:

Sister Nodes:

Absent ossification of thoracic vertebral bodies (HP:0012792)

Absent vertebral body mineralization (HP:0004605)

Poorly ossified vertebrae (HP:0100856)

Unossified vertebral bodies (HP:0004606)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005885	HP:0005885	Absent ossification of cervical vertebral bodies	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.