Fetal methylmercury syndrome
Synonyms: Congenital Minamata disease · Fetal methylmercury poisoning · Intrauterine methylmercury poisoning · Prenatal methylmercury poisoning
- Type
- Malformation syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal, Neonatal
- Status
- active
A toxic embryofetopathy characterized by a group of symptoms with unspecific neurologic involvement that may be observed in a foetus or newborn when the mother was exposed during pregnancy to excessive amounts of methylmercury.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Fetal methylmercury syndrome | Congenital Minamata disease · Fetal methylmercury poisoning · Intrauterine methylmercury poisoning · Prenatal methylmercury poisoning |
| fr | Embryopathie au méthylmercure | Exposition intrautérine au méthylmercure · Intoxication fétale au méthylmercure · Intoxication prénatale au méthylmercure · Maladie de Minamata congénitale |
| de | Methylquecksilber-Embryopathie | Methylquecksilber-Exposition, vorgeburtliche · Methylquecksilber-Vergiftung, pränatale · Minamata-Krankheit, kongenitale · Quecksilber-Exposition, vorgeburtliche |
| es | Síndrome del metilmercurio fetal | Enfermedad de Minamata congénita · Intoxicación fetal por metilmercurio · Intoxicación intrauterina por metilmercurio · Intoxicación prenatal por metilmercurio |
| it | Sindrome fetale da metilmercurio | Intossicazione fetale da metilmercurio · Intossicazione intrauterina da metilmercurio · Intossicazione prenatale da metilmercurio · Malattia di Minamata congenita |
| nl | Foetaal methylkwiksyndroom | Congenitale Minamata-ziekte · Foetale intoxicatie door methylkwik · Intra-uteriene intoxicatie door methylkwik · Prenatale intoxicatie door methylkwik |
| pt | Síndrome de metilmercúrio fetal | Doença Minamata congénita · Envenenamento fetal por metilmercúrio · Envenenamento intrauterino por metilmercúrio · Envenenamento prénatal por metilmercúrio |
| pl | Płodowy zespół metylortęciowy | Choroba Minamata · Prenatalne zatrucie metylortęcią |
| cs | Fetální metylrtuťový syndrom | Nemoc zálivu Minamata |
| uk | Фетальний метилртутний синдром | Вроджена хвороба Мінамата · Отруєння плоду метилртуттю · Внутрішньоутробне отруєння метилртуттю · Пренатальне отруєння метилртуттю |
| zh | 胎儿甲基汞综合征 | 产前甲基汞感染 |
| tr | Fetal metil cıva sendromu | Minamata hastalığı · Metil cıva antenatal enfeksiyon |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | T56.1 | NTBT | attributed | validated |
| ICD-11 | LD2F.0Y | NTBT | index | validated |
| MONDO | 0016013 | E | validated | |
| UMLS | C0265376 | E | validated | |
| GARD | 3575 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:138059Teratogenic Pierre Robin syndrome
rare developmental anomalies during embryogenesis; rare otorhinolaryngological diseases; rare surgical maxillo-facial diseases - ORPHA:251529Toxic or drug-related embryofetopathy
rare developmental anomalies during embryogenesis; rare disorders due to toxic effects; rare teratologic disorders
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | 34881051[PMID]_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.
HPO phenotypes
5 annotations · validated 2016-06-01| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0000365 | Hearing impairment | |
| HP:0001252 | Hypotonia | |
| HP:0000252 | Microcephaly | |
| HP:0004322 | Short stature | |
| HP:0000505 | Visual impairment | |
Run the differential on the 5 obligate / very frequent terms
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/1917
- This record as JSON: /data/d/1917.json