Search for a rare disease

* (*) mandatory field

Other search option(s)

Suggest an update

(*) Required fields.


Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. For all other comments, please send your remarks via contact us. Only comments written in English can be processed.

Captcha image

Orofaciodigital syndrome type 6

Disease definition

Joubert syndrome with orofaciodigital defect (or oral-facial-digital syndrome type 6, OFD6) is a very rare subtype of Joubert syndrome and related disorders (JSRD, see this term) characterized by the neurological features of JS associated with orofacial anomalies and often polydactyly.


Classification level: Disorder
  • Synonym(s):
    • Joubert syndrome with oral-facial-digital syndrome
    • Joubert syndrome with orofaciodigital defect
    • OFD6
    • Oral-facial-digital syndrome type 6
    • Polydactyly-cleft lip/palate-psychomotor retardation syndrome
    • Váradi syndrome
    • Váradi-Papp syndrome
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive or X-linked recessive 
  • Age of onset: Infancy, Neonatal
  • ICD-10: Q04.3
  • OMIM: 277170  300804  614815  615665  617127
  • UMLS: C2745997
  • MeSH: -
  • GARD: 4412
  • MedDRA: -

Detailed information


The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.