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 male germ cell morphology (HP:0012863)

Parent Node:
Abnormal sperm morphology (HP:0012864)

..Starting node
..Abnormal sperm neck morphology (HP:0012866)

Term ID:

12866

Name:

Abnormal sperm neck morphology

Synonym:

Sperm neck anomaly

Definition:

A structural abnormality of the sperm neck.

Comments:

Reference:

HP:0012866

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal sperm head morphology (HP:0012865)

Abnormal sperm mid-piece morphology (HP:0012867)

Abnormal sperm tail morphology (HP:0012868)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012866	HP:0012866	Abnormal sperm neck morphology	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.