Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Abnormalities of placenta or umbilical cord (HP:0001194)

Parent Node:
Abnormal placenta morphology (HP:0100767)

..Starting node
..Placental abruption (HP:0011419)

Term ID:

11419

Name:

Placental abruption

Synonym:

Abruptio placentae

Definition:

Separation of the placenta from the uterus wall before delivery.

Comments:

Reference:

HP:0011419

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal placental size (HP:0012767)

Calcified placenta (HP:0011415)

Chorangioma (HP:0100883)

Choriocarcinoma (HP:0100768)

Placental infarction (HP:0011416)

Subchorionic septal cyst (HP:0030720)

Subchorionic thrombohematoma (HP:0030714)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011419	HP:0011419	Placental abruption	0	CD46 CL E G H	4179	6953	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional	39
HP:0011419	HP:0011419	Placental abruption	0	CFH CL E G H	3075	4883	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional	86
HP:0011419	HP:0011419	Placental abruption	0	CFI CL E G H	3426	5394	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional	57
HP:0011419	HP:0011419	Placental abruption	0	FANCF CL E G H	2188	3587	OMIM:603467	FANCONI ANEMIA, COMPLEMENTATION GROUP F; FANCF		87
HP:0011419	HP:0011419	Placental abruption	0	HELLPAR CL E G H	101101692	43984	ORPHA:244242	HELLP syndrome	HP:0040283 - Occasional

Genes (5) :CD46 CFH CFI FANCF HELLPAR

Diseases (2) :ORPHA:244242 OMIM:603467

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