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:
Abnormality of the umbilical cord (HP:0010881)

Parent Node:
Abnormal insertion of umbilical cord (HP:0011418)

..Starting node
..Velamentous cord insertion (HP:0030659)

Term ID:

30659

Name:

Velamentous cord insertion

Synonym:

Definition:

Insertion of the umbilical cord into the chorio-amniotic membranes of the placenta.

Comments:

Reference:

HP:0030659

Genes and Diseases:

Child Nodes:

Sister Nodes:

Furcate cord insertion (HP:0030660)

Marginal umbilical cord insertion (HP:0030658)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030659	HP:0030659	Velamentous cord insertion	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.