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 nervous system physiology (HP:0012638)

Parent Node:
Abnormality of intracranial pressure (HP:0012640)

..Starting node
..Decreased intracranial pressure (HP:0012641)

Term ID:

12641

Name:

Decreased intracranial pressure

Synonym:

Intracranial hypotension

Definition:

A reduction of the pressure inside the cranium (skull) and thereby in the brain tissue and cerebrospinal fluid.

Comments:

Reference:

HP:0012641

Genes and Diseases:

Child Nodes:

Sister Nodes:

Increased intracranial pressure (HP:0002516)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012641	HP:0012641	Decreased intracranial pressure	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.