Human Phenotype Ontology 
Grandparent Node:
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Prenatal maternal abnormality (HP:0002686)help
Parent Node:
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Toxemia of pregnancy (HP:0100603)help
..Starting node
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Maternal hypertension (HP:0008071)help
Term ID: 8071
Name: Maternal hypertension
Synonym:
Definition: Increased blood pressure during a pregnancy.
Comments:
Reference: HP:0008071
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandEclampsia (HP:0100601) help
..expandPreeclampsia (HP:0100602) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0008071HP:0008071Maternal hypertension0ASH1L CL E G H5587019088OMIM:617796Mental retardation, autosomal dominant 521
HP:0008071HP:0008071Maternal hypertension0CD46 CL E G H41796953ORPHA:244242HELLP syndromeHP:0040282 - Frequent39
HP:0008071HP:0008071Maternal hypertension0CFH CL E G H30754883ORPHA:244242HELLP syndromeHP:0040282 - Frequent86
HP:0008071HP:0008071Maternal hypertension0CFI CL E G H34265394ORPHA:244242HELLP syndromeHP:0040282 - Frequent57
HP:0008071HP:0008071Maternal hypertension0HELLPAR CL E G H10110169243984ORPHA:244242HELLP syndromeHP:0040282 - Frequent
HP:0008071HP:0008071Maternal hypertension0NOS3 CL E G H48467876OMIM:189800Preeclampsia/eclampsia 1.8
HP:0008071HP:0008071Maternal hypertension0NR3C2 CL E G H43067979OMIM:605115Hypertension, early-onset, autosomal dominant, with severe exacerbationin pregnancy109
HP:0008071HP:0008071Maternal hypertension0SPTBN1 CL E G H671111275OMIM:619475DEVELOPMENTAL DELAY, IMPAIRED SPEECH, AND BEHAVIORAL ABNORMALITIES; DDISBA


Genes (8) :ASH1L CD46 CFH CFI HELLPAR NOS3 NR3C2 SPTBN1

Diseases (5) :OMIM:617796 ORPHA:244242 OMIM:189800 OMIM:605115 OMIM:619475
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.