Human Phenotype Ontology 
Grandparent Node:
expand
Abnormality of prenatal development or birth (HP:0001197)help
Parent Node:
expand
Abnormal bleeding (HP:0001892)help
Parent Node:
expand
Abnormal delivery (HP:0001787)help
..Starting node
..expand
Cephalohematoma (HP:0012541)help
Term ID: 12541
Name: Cephalohematoma
Synonym: Cephalohaematoma
Definition: Hemorrhage between the skull and periosteum of a newborn resulting from rupture of blood vessels that cross the periosteum.
Comments:
Reference: HP:0012541
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBreech presentation (HP:0001623) help
..expandCaesarian section (HP:0011410) 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:0012541HP:0012541Cephalohematoma0CD109 CL E G H13522821685ORPHA:853Fetal and neonatal alloimmune thrombocytopeniaHP:0040282 - Frequent
HP:0012541HP:0012541Cephalohematoma0CDC42BPB CL E G H95781738OMIM:619841
HP:0012541HP:0012541Cephalohematoma0F2 CL E G H21473535ORPHA:325Congenital factor II deficiencyHP:0040283 - Occasional44
HP:0012541HP:0012541Cephalohematoma0F8 CL E G H21573546ORPHA:169802Severe hemophilia AHP:0040283 - Occasional303
HP:0012541HP:0012541Cephalohematoma0GP1BA CL E G H28114439ORPHA:853Fetal and neonatal alloimmune thrombocytopeniaHP:0040282 - Frequent23
HP:0012541HP:0012541Cephalohematoma0GP1BB CL E G H28124440ORPHA:853Fetal and neonatal alloimmune thrombocytopeniaHP:0040282 - Frequent8
HP:0012541HP:0012541Cephalohematoma0ITGA2 CL E G H36736137ORPHA:853Fetal and neonatal alloimmune thrombocytopeniaHP:0040282 - Frequent119
HP:0012541HP:0012541Cephalohematoma0ITGA2B CL E G H36746138ORPHA:853Fetal and neonatal alloimmune thrombocytopeniaHP:0040282 - Frequent69
HP:0012541HP:0012541Cephalohematoma0ITGB3 CL E G H36906156ORPHA:853Fetal and neonatal alloimmune thrombocytopeniaHP:0040282 - Frequent80


Genes (9) :CD109 CDC42BPB F2 F8 GP1BA GP1BB ITGA2 ITGA2B ITGB3

Diseases (4) :ORPHA:853 OMIM:619841 ORPHA:325 ORPHA:169802
 

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