Human Phenotype Ontology 
Grandparent Node:
expandPhenotypic abnormality (HP:0000118)help
Parent Node:
expandAbnormality of prenatal development or birth (HP:0001197)help
..Starting node
..expandIntrauterine fetal demise of one twin after midgestation (HP:0030753)help
Term ID: 30753
Name: Intrauterine fetal demise of one twin after midgestation
Synonym: Intrauterine foetal demise of one twin after midgestation; Single-twin demise
Definition: Loss of one twin occurring after midgestation (17 weeks gestation).
Comments:
Reference: HP:0030753
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
..expandLow APGAR score (HP:0030917) help
..expandPostterm pregnancy (HP:0031169) 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:0030753HP:0030753Intrauterine fetal demise of one twin after midgestation0 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.