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:
Prenatal maternal abnormality (HP:0002686)

Parent Node:
Abnormal maternal serum screening (HP:0011436)

..Starting node
..High maternal circulating chorionic gonadotropin concentration (HP:0011433)

Term ID:

11433

Name:

High maternal circulating chorionic gonadotropin concentration

Synonym:

High maternal serum chorionic gonadotropin; High maternal serum hCG

Definition:

An abnormally high concentration of maternal serum human chorionic gonadotropin as compared to normal values for gestational-age.

Comments:

Reference:

HP:0011433

Genes and Diseases:

Child Nodes:

Sister Nodes:

High maternal circulating alpha-fetoprotein concentration (HP:0011432)

Low maternal circulating alpha-fetoprotein concentration (HP:0010570)

Low maternal circulating chorionic gonadotropin concentration (HP:0011434)

Low maternal circulating estriol concentration (HP:0008073)

Low maternal circulating PAPP-A concentration (HP:0011435)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011433	HP:0011433	High maternal circulating chorionic gonadotropin concentration	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.