ORPHA:180766

Malformative syndrome with dentinogenesis imperfecta

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.

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Malformative syndrome with dentinogenesis imperfecta
fr	Syndrome malformatif avec dentinogenèse imparfaite
de	Fehlbildungssyndrom mit Dentinogenesis imperfecta
es	Síndrome malformativo con dentinogénesis imperfecta
it	Sindrome malformativa con dentinogenesi imperfetta
nl	Malformatief syndroom met dentinogenesis imperfecta
pt	Síndrome malformativo com dentinogénese imperfeita
pl	Zespół wad wrodzonych z dentinogenesis imperfecta
cs	Malformační syndrom s dentinogenesis imperfecta
uk	Мальформативний синдром з недосконалим дентиногенезом
zh	伴牙本质发育不全的畸形综合征
tr	Dentinogenesis imperfekta ile seyreden malformatif sendrom

Cross-references

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
MONDO	15877	E		validated
UMLS	C5680472	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):

ORPHA:93890Rare developmental defect during embryogenesis

Parents in the classifications (2):

ORPHA:139042Malformation syndrome with odontal and/or periodontal component
rare developmental anomalies during embryogenesis; rare odontological diseases
ORPHA:77830Rare genetic odontologic disease
rare genetic diseases

Children (4):

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

Sources for this card

Orphanet page: orpha.net/en/disease/detail/180766
This record as JSON: /data/d/180766.json