PREGNANCY LOSS, RECURRENT, SUSCEPTIBILITY TO, 3

General Information (adopted from Orphanet):

Synonyms, Signs: RPRGL3
Number of Symptoms 2
OrphanetNr:
OMIM Id: 614391
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Autosomal dominant inheritance
[Omim]
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0200067) Recurrent spontaneous abortion 6 / 7739
2
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information:

Description: (OMIM) Miscarriage, the commonest complication of pregnancy, is the spontaneous loss of a pregnancy before the fetus has reached viability. The term therefore includes all pregnancy losses from the time of conception until 24 weeks of gestation. Recurrent miscarriage, ...
Molecular genetics OMIM In 70 German patients with recurrent pregnancy loss (RPRGL) who were known to carry neither factor V Leiden (612309.0001) nor the 20210G-A prothrombin mutation (176930.0009), Bogdanova et al. (2007) analyzed the gene encoding the placental anticoagulant protein annexin ...