Orofaciodigital syndrome or oral-facial-digital syndrome is a group of at least 13 related conditions that affect the development of the mouth, facial...
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Orofaciodigital syndrome 1 (OFD1), also called Papillon-Léage and Psaume syndrome, is an X-linked congenital disorder characterized by malformations of...
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syndrome Orofaciodigital syndrome Gabrielli type Orofaciodigital syndrome Shashi type Orofaciodigital syndrome Thurston type Orofaciodigital syndrome...
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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
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
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
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
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
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
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
Sugarman syndrome is the common name of autosomal recessive oral-facial-digital syndrome type III, one of ten distinct genetic disorders that involve...
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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...
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(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
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
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
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...
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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...
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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
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