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 white matter morphology (HP:0002500)

Parent Node:
Hypointensity of cerebral white matter on MRI (HP:0007103)

Parent Node:
Multifocal cerebral white matter abnormalities (HP:0007052)

..Starting node
..Multifocal hypointensity of cerebral white matter on MRI (HP:0040332)

Term ID:

40332

Name:

Multifocal hypointensity of cerebral white matter on MRI

Synonym:

Definition:

Comments:

Reference:

HP:0040332

Genes and Diseases:

Child Nodes:

Sister Nodes:

Multifocal hyperintensity of cerebral white matter on MRI (HP:0040329)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040332	HP:0040332	Multifocal hypointensity of cerebral white matter on MRI	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.