Human Phenotype Ontology 
Grandparent Node:
expandGrowth delay (HP:0001510)help
Parent Node:
expandIntrauterine growth retardation (HP:0001511)help
..Starting node
..expandMild intrauterine growth retardation (HP:0008883)help
Term ID: 8883
Name: Mild intrauterine growth retardation
Synonym: Mild prenatal growth deficiency
Definition: Intrauterine growth retardation that is at least 2 standard deviations (SD) below average, but not as low as 3 SD, corrected for sex and gestational age.
Comments:
Reference: HP:0008883
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandModerate intrauterine growth retardation (HP:0011408) help
..expandSevere intrauterine growth retardation (HP:0008846) 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:0008883HP:0008883Mild intrauterine growth retardation0GTF2E2 CL E G H29614651OMIM:616943Trichothiodystrophy 6, nonphotosensitive2
HP:0008883HP:0008883Mild intrauterine growth retardation0NSDHL CL E G H5081413398OMIM:308050Congenital hemidysplasia with ichthyosiform erythroderma and limb defects.34


Genes (2) :GTF2E2 NSDHL

Diseases (2) :OMIM:616943 OMIM:308050
 

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