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Differential Diagnosis For Snoring: Hereditary, Familial, Genetic Disorders

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List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Oromandibular facial dystonia syndrome
Cystic fibrosis (mucoviscidosis)
Fragile X syndrome/X-linked retardation
Jackson-Weiss Craniosynostosis syndrome
Johanson Blizzard genetic syndrome (unco)
Mitochondrial myopathy/MERRF
Beckwith-Wiedemann Syndrome
Pallister W Syndrome
Apert syndrome
Bird-headed dwarf of Seckel
Chondrodysplasia punctata/calcificans (Conradi)
Facial ectodermal dysplasia (Setleis)
Facioscapulohumeral muscular dystrophy
Klipple-Feil syndrome
Nemaline myopathy
Scott's Craniodigital syndrome
Simpson dysmorphia syndrome
Stickler syndrome
Treacher Collins syndrome
Williams syndrome/Elfin facies
18p chromosome deletion complex
Cowden disease/CD (10q23.31)
Craniofrontonasal Syndrome (CFNS)
Myopathy, Desmin Storage type/Sarcoplasmin bodies
Myopathy, Myotubular/Centronuclear
Neuhauser Syndrome
Orocraniodigital (Juberg-Hayward) Syndrome
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