• Thumbnail for Orofaciodigital syndrome
    Orofaciodigital syndrome or oral-facial-digital syndrome is a group of at least 13 related conditions that affect the development of the mouth, facial...
    3 KB (240 words) - 19:32, 12 June 2023
  • Thumbnail for Orofaciodigital syndrome 1
    Orofaciodigital syndrome 1 (OFD1), also called Papillon-Léage and Psaume syndrome, is an X-linked congenital disorder characterized by malformations of...
    7 KB (661 words) - 02:14, 3 December 2023
  • syndrome Orofaciodigital syndrome Gabrielli type Orofaciodigital syndrome Shashi type Orofaciodigital syndrome Thurston type Orofaciodigital syndrome...
    10 KB (818 words) - 01:37, 27 October 2023
  • syndrome Oral mite anaphylaxis Oral-facial-digital syndrome Orbital apex syndrome Organic brain syndrome Organic dust toxic syndrome Orofaciodigital syndrome...
    42 KB (4,065 words) - 03:07, 17 August 2024
  • Thumbnail for Tongue splitting
    with maternal diabetes, orofaciodigital syndrome 1, Ellis–Van Creveld syndrome, Goldenhar syndrome, and Klippel–Feil syndrome. Deliberate tongue splitting...
    12 KB (1,461 words) - 10:20, 18 June 2024
  • Thumbnail for Clinodactyly
    Lange syndrome Orofaciodigital syndrome 1 13q deletion syndrome XXYY syndrome Silver–Russell syndrome Andersen-Tawil syndrome Noonan syndrome Ehlers–Danlos...
    5 KB (498 words) - 15:05, 30 July 2024
  • Thumbnail for Hyperdontia
    Ehlers–Danlos syndrome Type III, Ellis–van Creveld syndrome, Gardner's syndrome, Goldenhar syndrome, Hallermann–Streiff syndrome, Orofaciodigital syndrome type...
    21 KB (2,487 words) - 14:29, 17 August 2024
  • Thumbnail for Trigonocephaly
    Trigonocephaly (redirect from C syndrome)
    dysostosis-microcephaly syndrome MEGF8-related Carpenter syndrome Microcephaly, primary autosomal dominant Mucolipidosis type II Orofaciodigital syndrome type 14 Paris-Trousseau...
    35 KB (3,636 words) - 03:36, 30 July 2024
  • Thumbnail for Ciliopathy
    disease, nephronophthisis, Senior–Løken syndrome type 5, orofaciodigital syndrome type 1 and Bardet–Biedl syndrome. Adams M, Smith UM, Logan CV, Johnson...
    35 KB (2,499 words) - 18:40, 12 July 2024
  • Thumbnail for Basal body
    diseases, including Bardet–Biedl syndrome, orofaciodigital syndrome, Joubert syndrome, cone-rod dystrophy, Meckel syndrome, and nephronophthisis. Regulation...
    12 KB (1,204 words) - 14:44, 23 August 2023
  • Thumbnail for Sugarman syndrome
    Sugarman syndrome is the common name of autosomal recessive oral-facial-digital syndrome type III, one of ten distinct genetic disorders that involve...
    2 KB (89 words) - 07:09, 6 November 2023
  • Department Ogof Ffynnon Ddu, an extensive cave system in South Wales Orofaciodigital syndrome One Fine Day (U.S. TV series), a 2007–2008 American Internet Protocol...
    593 bytes (109 words) - 13:35, 28 July 2024
  • Thumbnail for List of skin conditions
    (Delleman–Oorthuys syndrome) Oculodentodigital dysplasia Odonto–Tricho–Ungual–Digital–Palmar syndrome Oliver–McFarlane syndrome Orofaciodigital syndrome Pachydermoperiostosis...
    198 KB (17,958 words) - 01:24, 6 July 2024
  • Thumbnail for Micrognathism
    Ogden syndrome Orofacial cleft 13 Orofacial-digital syndrome IV Orofaciodigital syndrome types 6 and 14 Osteogenesis imperfecta types 3, 10, 12, and 18...
    14 KB (1,343 words) - 23:07, 26 April 2024
  • Thumbnail for Acrocallosal syndrome
    syndrome, orofaciodigital syndrome types I and II, Meckel–Gruber syndrome, Smith–Lemli–Opitz syndrome, Rubinstein–Taybi syndrome, Cockayne syndrome,...
    10 KB (939 words) - 15:13, 27 October 2023
  • Thumbnail for Acrocephalosyndactyly
    Crouzon-Pfeiffer syndrome. Acrocephalosyndactyly type IV was formerly called Mohr Syndrome, however, it was later classified under Orofaciodigital syndrome type II...
    30 KB (2,746 words) - 02:29, 7 July 2024
  • hepatic defect Orofaciodigital syndrome type 6 Joubert syndrome with ocular defect Joubert syndrome with renal defect Joubert syndrome with Jeune asphyxiating...
    4 KB (426 words) - 16:52, 8 April 2023
  • cystic kidney disease Jeune syndrome Nephronophthisis Meckel–Gruber syndrome Orofaciodigital syndrome Zellweger syndrome In addition, GCKD can be a component...
    11 KB (1,406 words) - 07:57, 8 June 2024
  • Syndromic microphthalmia is a class of rare congenital anomalies characterized by microphthalmia along with other non-ocular malformations. Syndromic...
    13 KB (538 words) - 09:46, 18 March 2024
  • oculocerebrorenal syndrome MeSH C16.131.077.677 – orofaciodigital syndromes MeSH C16.131.077.703 – POEMS syndrome MeSH C16.131.077.730 – Prader–Willi syndrome MeSH C16...
    78 KB (6,496 words) - 05:23, 12 April 2022
  • Ehlers–Danlos syndrome COL5A2 Collagen type 5 Classic variant of Ehlers–Danlos syndrome CTNNB1 Beta-catenin Pilomatricoma CX0RF5 Orofaciodigital syndrome CYLD...
    12 KB (108 words) - 02:46, 17 September 2022
  • syndrome MeSH C05.116.099.370.652 – orofaciodigital syndromes MeSH C05.116.099.370.797 – Rubinstein–Taybi syndrome MeSH C05.116.099.370.894 – synostosis...
    35 KB (2,265 words) - 16:55, 9 February 2024
  • Thumbnail for OFD1
    chromosomal rearrangements.[supplied by OMIM] Orofaciodigital syndrome 1 Simpson–Golabi–Behmel syndrome GRCh38: Ensembl release 89: ENSG00000046651 –...
    7 KB (923 words) - 22:10, 4 September 2022