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 ulnar epiphysis morphology (HP:0004037)

Parent Node:
Abnormal ulnar styloid process morphology (HP:0004035)

..Starting node
..Absent styloid process of ulna (HP:0005068)

Term ID:

5068

Name:

Absent styloid process of ulna

Synonym:

Definition:

Comments:

Reference:

HP:0005068

Genes and Diseases:

Child Nodes:

Sister Nodes:

Long styloid process of ulna (HP:0004036)

Prominent styloid process of ulna (HP:0004981)

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:0005068	HP:0005068	Absent styloid process of ulna	0	COL2A1 CL E G H	1280	2200	OMIM:271700	Spondyloperipheral dysplasia	.	284

Genes (1) :COL2A1

Diseases (1) :OMIM:271700

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