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 prenatal development or birth (HP:0001197)

Grandparent Node:
Edema (HP:0000969)

Parent Node:
Hydrops fetalis (HP:0001789)

..Starting node
..obsolete Severe hydrops fetalis (HP:0005099)

Term ID:

5099

Name:

obsolete Severe hydrops fetalis

Synonym:

Severe hydrops

Definition:

Comments:

Reference:

HP:0005099

Genes and Diseases:

Child Nodes:

Sister Nodes:

Nonimmune hydrops fetalis (HP:0001790)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0005099	HP:0005099	obsolete Severe hydrops fetalis	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.