raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:3013

Radiculomegaly of canine teeth- congenital cataract

inactive · moved to ORPHA:2712Oculofaciocardiodental syndrome

Synonyms: Marashi-Gorlin syndrome

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Oculofaciocardiodental syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRadiculomegaly of canine teeth- congenital cataractMarashi-Gorlin syndrome
frSyndrome de radiculomégalie des canines-cataracte congénitaleSyndrome de Marashi-Gorlin
deRadikulomegalie der Eckzähne - kongenitale KataraktMarashi-Gorlin-Syndrom
esRadiculomegalia de caninos-cataratas congénitasSíndrome de Marashi-Gorlin
itRadiculomegalia dei canini - cataratta congenitaSindrome di Marashi-Gorlin
nlRadiculomegalie van hoektanden - congenitaal cataractSyndroom van Marashi-Gorlin
ptRadiculomegalia dos dentes caninos-catarata congénitaSíndrome Marashi-Gorlin
plRadikulomegalia kłów - zaćma wrodzonaZespół Marashi i Gorlina
csRadikulomegalie špičáků a vrozená kataraktaMarashiho-Gorlinův syndrom · Marashi-Gorlinův syndrom
ukРадикуломегалія іклів - вроджена катарактаСиндром Мараші-Горліна
zh尖牙牙根肥大-先天性白内障Marashi-Gorlin综合征
trKöpek dişlerinin radikülomegalisi - Doğumsal kataraktMarashi-Gorlin sendromu
2

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

3

Classification

Not placed in any Orphanet classification in this release.

No children.

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