raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:156202

Otomandibular dysplasia associated with monogenic syndromes

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
LangNameSynonyms
enOtomandibular dysplasia associated with monogenic syndromes
frDysplasie oto-mandibulaire des syndromes monogéniques
deDysplasie, otomandibuläre, mit assoziierten monogenetischen Syndromen
esDisplasia otomandibular asociada con síndromes monogénicos
itDisplasia oto-mandibolare associata a sindromi monogeniche
nlOtomandibulaire dysplasie geassocieerd met monogene syndromen
ptDisplasia otomandibular como parte de síndromes monogénicos
plDysplazja uszno-żuchwowa związana z zespołami monogenowymi
csOtomandibulární dysplázie asociovaná s monogenními syndromy
ukОтомандибулярна дисплазія, повязана з моногенними синдромами
zh单基因综合征相关耳下颌骨综合征
trMonojenik sendromları -ilişkili otomandibular displazi
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO15495Evalidated
UMLSC5680668Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

  • ORPHA:155896Otomandibular dysplasia
    rare developmental anomalies during embryogenesis; rare genetic diseases; rare bone diseases; rare otorhinolaryngological diseases; rare surgical maxillo-facial diseases

Children (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card