ORPHA:163637
Rare disorder related with pregnancy, childbirth and puerperium
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder related with pregnancy, childbirth and puerperium | |
| fr | Maladie rare liée à la grossesse et à la périnatalité | |
| de | Seltene Krankheit in Verbindung mit Schwangerschaft, Geburt und Wochenbett | |
| es | Trastornos raros relacionados con embarazo, nacimiento y puerperio | |
| it | Malattia rara associata a gravidanza, parto e puerperio | |
| nl | Zeldzame stoornis gerelateerd aan zwangerschap, bevalling en kraambedperiode | |
| pt | Doença rara relacionada com gravidez, parto e puerpério | |
| pl | Rzadkie schorzenie związane z ciążą, porodem lub połogiem | |
| cs | Vzácná onemocnění související s těhotenstvím, porodem a šestinedělím | |
| uk | Рідкісний розлад, повязаний з вагітністю, пологами та післяпологовим періодом | |
| zh | 妊娠、分娩和产褥期相关罕见疾病 | |
| tr | Gebelik, doğum ve lohusalık ilişkili nadir bozukluk |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15582 | E | validated | |
| UMLS | C5680447 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:96344Rare gynecologic or obstetric disease
rare gynecological and obstetric diseases
Children (20):
- ORPHA:243367Acute fatty liver of pregnancy
- ORPHA:617304Amniotic fluid embolism
- ORPHA:80Antiphospholipid syndrome
- ORPHA:91Aromatase deficiency
- ORPHA:615970Chronic intervillositis of unknown etiology
- ORPHA:99819Familial gestational hyperthyroidism
- ORPHA:244242HELLP syndrome
- ORPHA:88660Hypertension due to gain-of-function mutations in the mineralocorticoid receptor
- ORPHA:647823Idiopathic pregnancy-associated osteoporosis
- ORPHA:69665Intrahepatic cholestasis of pregnancy
- ORPHA:289385Malignancy diagnosed during pregnancy
- ORPHA:563Peripartum cardiomyopathy
- ORPHA:662721Placenta accreta spectrum disorder
- ORPHA:439167Placental insufficiency
- ORPHA:443173Postpartum psychosis
- ORPHA:275555Preeclampsia
- ORPHA:723290Pregnancy-associated spontaneous coronary artery dissection
- ORPHA:64745Pruritic urticarial papules and plaques of pregnancy
- ORPHA:617307Rare disorder related to monochorionic twin pregnancy
- ORPHA:662786Vasa previa
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/163637
- This record as JSON: /data/d/163637.json