Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Abnormality of the abdominal organs (HP:0002012)

Parent Node:
Abnormality of mesentery morphology (HP:0100016)

..Starting node
..Mesenteric cyst (HP:0030451)

Term ID:

30451

Name:

Mesenteric cyst

Synonym:

Definition:

A closed fluid filled sac originating from the mesentary.

Comments:

Reference:

HP:0030451

Genes and Diseases:

Child Nodes:

........

Chylolymphatic mesenteric cyst (HP:0030452)

Sister Nodes:

Peritoneal mesothelioma (HP:0100003)

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:0030451	HP:0030451	Mesenteric cyst	0	TMEM94 CL E G H	9772	28983	OMIM:618316	Intellectual developmental disorder with cardiac defects and dysmorphic facies	1
HP:0030451	HP:0030452	Chylolymphatic mesenteric cyst	1	CL E G H

Genes (1) :TMEM94

Diseases (1) :OMIM:618316

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