ORPHA:292
Congenital enterovirus infection
Synonyms: Antenatal enterovirus infection · Mother-to-child transmission of enterovirus infection
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal, Neonatal
- Status
- active
An infectious embryofetopathy including coxsackie viruses and ECHO viruses that have been reported to cause spontaneous abortion, stillbirth, acute systemic illness in the newborn, and possibly fetal malformations.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital enterovirus infection | Antenatal enterovirus infection · Mother-to-child transmission of enterovirus infection |
| fr | Infection congénitale à entérovirus | Infection anténatale aux entérovirus |
| de | Enterovirus-Infektion, kongenitale | Enteroviren-Infektion, vorgeburtliche · Enterovirus-Infektion durch Mutter-Kind-Übertragung · Enterovirus-Infektion, pränatale |
| es | Infección congénita por enterovirus | Infección prenatal por enterovirus · Transmisión materna de infección por enterovirus · Transmisión materna de la infección por enterovirus |
| it | Infezione congenita da enterovirus | Infezione prenatale da enterovirus |
| nl | Congenitale infectie door enterovirus | Prenatale infectie door enterovirus · Transmissie van moeder op kind van enterovirusinfectie |
| pt | Infeção congénita por Enterovírus | Infeção pré-natal por Enterovírus |
| pl | Wrodzone zakażenie enterowirusem | Prenatalne zakażenie enterowirusem |
| cs | Vrozená enterovirová infekce | Antenatální enterovirová infekce |
| uk | Вроджена ентеровірусна інфекція | Антенатальна ентеровірусна інфекція · Передача ентеровірусної інфекції від матері до дитини |
| zh | 先天性肠病毒感染 | 母婴传播的肠道病毒感染 |
| tr | Doğumsal enterovirüs enfeksiyonu | Antenatal enterovirüs enfeksiyonu · Enterovirüs enfeksiyonunun anneden çocuğa bulaşması |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | P35.8 | NTBT | attributed | validated |
| ICD-11 | KA62.5 | E | specific | validated |
| MONDO | 0017375 | E | validated | |
| UMLS | C4274223 | E | validated | |
| GARD | 2130 | 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:232035Infectious embryofetopathy
rare developmental anomalies during embryogenesis; rare infectious diseases; rare teratologic disorders
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
39 annotations · validated 2019-10-31| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000988 | Skin rash | |
| Frequent (79-30%) | ||
| HP:0025031 | Abnormality of the digestive system | |
| HP:0000707 | Abnormality of the nervous system | |
| HP:0002086 | Abnormality of the respiratory system | |
| HP:0001945 | Fever | |
| HP:0000737 | Irritability | |
| HP:0001287 | Meningitis | |
| HP:0100806 | Sepsis | |
| HP:0001873 | Thrombocytopenia | |
| Occasional (29-5%) | ||
| HP:0001892 | Abnormal bleeding | |
| HP:0011121 | Abnormal skin morphology | |
| HP:0001903 | Anemia | |
| HP:0200149 | CSF lymphocytic pleiocytosis | |
| HP:0001638 | Cardiomyopathy | |
| HP:0001396 | Cholestasis | |
| HP:0001558 | Decreased fetal movement | |
| HP:0001875 | Decreased total neutrophil count | |
| HP:0005521 | Disseminated intravascular coagulation | |
| HP:0001791 | Fetal ascites | |
| HP:0025116 | Fetal distress | |
| HP:0001399 | Hepatic failure | |
| HP:0012115 | Hepatitis | |
| HP:0001789 | Hydrops fetalis | |
| HP:0003073 | Hypoalbuminemia | |
| HP:0002615 | Hypotension | |
| HP:0001974 | Increased total leukocyte count | |
| HP:0002383 | Infectious encephalitis | |
| HP:0001882 | Leukopenia | |
| HP:0012819 | Myocarditis | |
| HP:0012758 | Neurodevelopmental delay | |
| HP:0001698 | Pericardial effusion | |
| HP:0002202 | Pleural effusion | |
| HP:0001561 | Polyhydramnios | |
| HP:0001622 | Premature birth | |
| HP:0002098 | Respiratory distress | |
| HP:0002119 | Ventriculomegaly | |
| Very rare (<4-1%) | ||
| HP:0004311 | Abnormal macrophage morphology | |
| HP:0001987 | Hyperammonemia | |
| HP:0002045 | Hypothermia | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 25126719[PMID]_28373042[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/292
- This record as JSON: /data/d/292.json