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 meningeal morphology (HP:0010651)

Grandparent Node:
Abnormality of the spinal cord (HP:0002143)

Parent Node:
Abnormal spinal meningeal morphology (HP:0010303)

..Starting node
..Spinal meningeal diverticulum (HP:0010304)

Term ID:

10304

Name:

Spinal meningeal diverticulum

Synonym:

Definition:

An outpouching of the spinal meninges.

Comments:

Reference:

HP:0010304

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal spinal dura mater morphology (HP:0009744)

Dural ectasia (HP:0100775)

Spinal arachnoid cyst (HP:0009745)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010304	HP:0010304	Spinal meningeal diverticulum	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.