Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Aplasia/Hypoplasia of the vertebrae (HP:0008515)

Parent Node:
Vertebral hypoplasia (HP:0008417)

..Starting node
..Posterior vertebral hypoplasia (HP:0008451)

Term ID:

8451

Name:

Posterior vertebral hypoplasia

Synonym:

Definition:

Comments:

Reference:

HP:0008451

Genes and Diseases:

Child Nodes:

Sister Nodes:

Central vertebral hypoplasia (HP:0008463)

Hypoplastic 5th lumbar vertebrae (HP:0008424)

Hypoplastic cervical vertebrae (HP:0008434)

Hypoplastic coccygeal vertebrae (HP:0008447)

Hypoplastic sacral vertebrae (HP:0008475)

Hypoplastic vertebral bodies (HP:0008479)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008451	HP:0008451	Posterior vertebral hypoplasia	0	COL11A1 CL E G H	1301	2186	OMIM:228520	Fibrochondrogenesis 1	.	215

Genes (1) :COL11A1

Diseases (1) :OMIM:228520

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.