Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of prenatal development or birth (HP:0001197)help
Parent Node:
expand
Abnormal delivery (HP:0001787)help
..Starting node
..expand
Caesarian section (HP:0011410)help
Term ID: 11410
Name: Caesarian section
Synonym: Caesarian section
Definition: Delivery of a fetus through surgical incisions made through the abdominal wall (laparotomy) and the uterine wall (hysterotomy).
Comments:
Reference: HP:0011410
Genes and Diseases:
 
       Child Nodes:
........expandPrimary Caesarian section (HP:0030363) help
........expandSecondary Caesarian section (HP:0030364) help

 Sister Nodes: 
..expandBreech presentation (HP:0001623) help
..expandCephalohematoma (HP:0012541) help
..expandDelivery by Odon device (HP:0030366) help
..expandForceps delivery (HP:0011411) help
..expandInduced vaginal delivery (HP:0030369) help
..expandMiscarriage (HP:0005268) help
..expandNuchal cord (HP:0012498) help
..expandPremature rupture of membranes (HP:0001788) help
..expandShoulder dystocia (HP:0011413) help
..expandTherapeutic abortion (HP:0030449) help
..expandVaginal birth after Caesarian (HP:0030365) help
..expandVentouse delivery (HP:0011412) 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:0011410HP:0011410Caesarian section0AGTPBP1 CL E G H2328717258OMIM:618276Neurodegeneration, childhood-onset, with cerebellar atrophy1
HP:0011410HP:0011410Caesarian section0ARSB CL E G H411714OMIM:253200Mucopolysaccharidosis, type VI120
HP:0011410HP:0011410Caesarian section0ASXL3 CL E G H8081629357OMIM:615485BAINBRIDGE-ROPERS SYNDROME; BRPS49
HP:0011410HP:0011410Caesarian section0CACNA1D CL E G H7761391ORPHA:369929Primary hyperaldosteronism-seizures-neurological abnormalities syndromeHP:0040282 - Frequent51
HP:0011410HP:0011410Caesarian section0CYP11B1 CL E G H15842591ORPHA:403Familial hyperaldosteronism type IHP:0040283 - Occasional112
HP:0011410HP:0011410Caesarian section0CYP11B2 CL E G H15852592ORPHA:403Familial hyperaldosteronism type IHP:0040283 - Occasional73
HP:0011410HP:0011410Caesarian section0MCM4 CL E G H41736947OMIM:609981Immunodeficiency 5469
HP:0011410HP:0011410Caesarian section0MTM1 CL E G H45347448OMIM:310400Myopathy, centronuclear, X-linked185
HP:0011410HP:0011410Caesarian section0OPA1 CL E G H49768140OMIM:616896MITOCHONDRIAL DNA DEPLETION SYNDROME 14 (CARDIOENCEPHALOMYOPATHIC TYPE); MTDPS14214
HP:0011410HP:0011410Caesarian section0POLR3A CL E G H1112830074ORPHA:3455Wiedemann-Rautenstrauch syndromeHP:0040282 - Frequent138
HP:0011410HP:0011410Caesarian section0PTCD3 CL E G H5503724717OMIM:619057COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 51; COXPD51
HP:0011410HP:0011410Caesarian section0SATB1 CL E G H630410541OMIM:619229KOHLSCHUTTER-TONZ SYNDROME-LIKE; KTZSL
HP:0011410HP:0011410Caesarian section0TAF1 CL E G H687211535OMIM:300966MENTAL RETARDATION, X-LINKED, SYNDROMIC 33; MRXS3321
HP:0011410HP:0011410Caesarian section0TAOK1 CL E G H5755129259OMIM:619575DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB
HP:0011410HP:0030363Primary Caesarian section1 CL E G H
HP:0011410HP:0030364Secondary Caesarian section1 CL E G H


Genes (14) :AGTPBP1 ARSB ASXL3 CACNA1D CYP11B1 CYP11B2 MCM4 MTM1 OPA1 POLR3A PTCD3 SATB1 TAF1 TAOK1

Diseases (13) :OMIM:618276 OMIM:253200 OMIM:615485 ORPHA:369929 ORPHA:403 OMIM:609981 OMIM:310400 OMIM:616896 ORPHA:3455 OMIM:619057 OMIM:619229 OMIM:300966 OMIM:619575
 

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