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:
Phenotypic abnormality (HP:0000118)

Parent Node:
Abnormality of the nervous system (HP:0000707)

..Starting node
..Abnormality of ganglion (HP:0410014)

Term ID:

410014

Name:

Abnormality of ganglion

Synonym:

Definition:

An abnormality of nerve cell cluster or a group of nerve cell bodies located in the autonomic nervous system.

Comments:

Reference:

HP:0410014

Genes and Diseases:

Child Nodes:

........

Abnormality of ganglion of peripheral nervous system (HP:0410015)

........

Abnormality of cranial ganglion (HP:0410016)

................... HP:3000025 Abnormality of ciliary ganglion

Sister Nodes:

Abnormal nervous system morphology (HP:0012639)

Abnormal nervous system physiology (HP:0012638)

Abnormality of the peripheral nervous system (HP:0410008)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410014	HP:0410014	Abnormality of ganglion	0	CL E G H
HP:0410014	HP:0410015	Abnormality of ganglion of peripheral nervous system	1	CL E G H
HP:0410014	HP:0410016	Abnormality of cranial ganglion	1	CL E G H
HP:0410014	HP:3000025	Abnormality of ciliary ganglion	2	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.