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:
Edema (HP:0000969)

Parent Node:
Intestinal edema (HP:0005225)

Parent Node:
Lymphedema (HP:0001004)

..Starting node
..Intestinal lymphedema (HP:0004788)

Term ID:

4788

Name:

Intestinal lymphedema

Synonym:

Definition:

Fluid retention and edema in the intestine caused by a compromised lymphatic system.

Comments:

Reference:

HP:0004788

Genes and Diseases:

Child Nodes:

Sister Nodes:

Predominantly lower limb lymphedema (HP:0003550)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004788	HP:0004788	Intestinal lymphedema	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.