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 cerebral ventricle morphology (HP:0002118)

Grandparent Node:
Abnormal cerebrospinal fluid morphology (HP:0002921)

Parent Node:
Hydrocephalus (HP:0000238)

..Starting node
..Severe hydrocephalus (HP:0006882)

Term ID:

6882

Name:

Severe hydrocephalus

Synonym:

Definition:

Comments:

Reference:

HP:0006882

Genes and Diseases:

Child Nodes:

Sister Nodes:

Communicating hydrocephalus (HP:0001334)

Noncommunicating hydrocephalus (HP:0010953)

Normal pressure hydrocephalus (HP:0002343)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006882	HP:0006882	Severe hydrocephalus	0	HYLS1 CL E G H	219844	26558	OMIM:236680	Hydrolethalus syndrome 1	31

Genes (1) :HYLS1

Diseases (1) :OMIM:236680

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