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:
Abnormalities of placenta or umbilical cord (HP:0001194)

Parent Node:
Abnormal placenta morphology (HP:0100767)

..Starting node
..Calcified placenta (HP:0011415)

Term ID:

11415

Name:

Calcified placenta

Synonym:

Placental calcification

Definition:

Comments:

Reference:

HP:0011415

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal placental size (HP:0012767)

Chorangioma (HP:0100883)

Choriocarcinoma (HP:0100768)

Placental abruption (HP:0011419)

Placental infarction (HP:0011416)

Subchorionic septal cyst (HP:0030720)

Subchorionic thrombohematoma (HP:0030714)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011415	HP:0011415	Calcified placenta	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.