Human Phenotype Ontology 
Grandparent Node:
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Phenotypic abnormality (HP:0000118)help
Parent Node:
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Abnormality of prenatal development or birth (HP:0001197)help
..Starting node
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Postterm pregnancy (HP:0031169)help
Term ID: 31169
Name: Postterm pregnancy
Synonym:
Definition: A pregnancy that extends to 42 weeks of gestation or beyond.
Comments:
Reference: HP:0031169
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal delivery (HP:0001787) help
..expandAbnormalities of placenta or umbilical cord (HP:0001194) help
..expandAbnormality of the amniotic fluid (HP:0001560) help
..expandFemale fetal virilization (HP:0031170) help
..expandFetal ascites (HP:0001791) help
..expandFetal distress (HP:0025116) help
..expandFetal ultrasound soft marker (HP:0011425) help
..expandHydrops fetalis (HP:0001789) help
..expandIncreased nuchal translucency (HP:0010880) help
..expandIntrauterine fetal demise of one twin after midgestation (HP:0030753) help
..expandLow APGAR score (HP:0030917) help
..expandPremature birth (HP:0001622) help
..expandPrenatal maternal abnormality (HP:0002686) help
..expandPrenatal movement abnormality (HP:0001557) help
..expandTwin-to-twin transfusion (HP:0031110) 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:0031169HP:0031169Postterm pregnancy0DUOX2 CL E G H5050613273ORPHA:226316Genetic transient congenital hypothyroidismHP:0040283 - Occasional121
HP:0031169HP:0031169Postterm pregnancy0MAGEL2 CL E G H545516814ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent63
HP:0031169HP:0031169Postterm pregnancy0MAGEL2 CL E G H545516814ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040283 - Occasional63
HP:0031169HP:0031169Postterm pregnancy0MAGEL2 CL E G H545516814ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040283 - Occasional63
HP:0031169HP:0031169Postterm pregnancy0NDN CL E G H46927675ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent
HP:0031169HP:0031169Postterm pregnancy0NDN CL E G H46927675ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040283 - Occasional
HP:0031169HP:0031169Postterm pregnancy0NDN CL E G H46927675ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040283 - Occasional
HP:0031169HP:0031169Postterm pregnancy0OCA2 CL E G H49488101ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent121
HP:0031169HP:0031169Postterm pregnancy0OCA2 CL E G H49488101ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040283 - Occasional121
HP:0031169HP:0031169Postterm pregnancy0OCA2 CL E G H49488101ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040283 - Occasional121
HP:0031169HP:0031169Postterm pregnancy0SNRPN CL E G H663811164ORPHA:98754Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15HP:0040282 - Frequent37
HP:0031169HP:0031169Postterm pregnancy0SNRPN CL E G H663811164ORPHA:177901Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1HP:0040283 - Occasional37
HP:0031169HP:0031169Postterm pregnancy0SNRPN CL E G H663811164ORPHA:177904Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2HP:0040283 - Occasional37


Genes (5) :DUOX2 MAGEL2 NDN OCA2 SNRPN

Diseases (4) :ORPHA:226316 ORPHA:98754 ORPHA:177901 ORPHA:177904
 

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