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Differential Diagnosis For Facies particular: Hereditary, Familial, Genetic Disorders


List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Basal cell nevus syndrome (Gorlin)
Cleidocranial digital dysostosis
Fragile X syndrome/X-linked retardation
Jackson-Weiss Craniosynostosis syndrome
Johanson Blizzard genetic syndrome (unco)
Juberg Marsidi Genetic syndrome (unco)
Pitt syndrome (4p16.3)
Pallister Hall Syndrome
Pallister W Syndrome
Zellweger Cerebrhepatorenal syndrome
Acrocephalosyndactyly type III syndrome
Bird-headed dwarf of Seckel
Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3)
Cockayne syndrome
Cryptophthalmos (Fraser) syndrome
Dolichospondylic dysplasia
Facial ectodermal dysplasia (Setleis)
Facioscapulohumeral muscular dystrophy
Lipodystrophy, generalized
Myotonia atrophica (Steinert's disease)
Oculocerebrorenal dystrophy/Lowe syndrome
Osteodysplasia, familial (Melnick Needles)
Schwartz-Jampel syndrome
Scott's Craniodigital syndrome
SHORT syndrome (Rieger anomaly plus)
Simpson dysmorphia syndrome
Smith-Lemli-Opitz syndrome
Stickler syndrome
Treacher Collins syndrome
Waardenburg-Klein syndrome
Williams syndrome/Elfin facies
Andermann Syndrome
Brooks syndrome
Segawa Syndrome/Infant Parkinsonism