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Possible Causes For Mental retardation - Causes: Hereditary, Familial, Genetic Disorders

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List of current finding(s):

Hereditary, Familial, Genetic Disorders: next: Degenerative-Age Related Causes
Xeroderma/Dry skin
Hemoglobin H disease
Ataxia-telangiectasia
Cleidocranial digital dysostosis
Duchenne's Muscular Dystrophy/Pseudohypertrophic
Fragile X syndrome/X-linked retardation
Infantile neuroaxonal dystrophy
Nephritis, hereditary (Alports)
Neurofibromatosis
Paraplegia, spastic hereditary
Pseudo-pseudohypoparathyroidism
Tuberous Sclerosis
Chromosome 22q13.3 deletion syndrome (22q13.3)
Johanson Blizzard genetic syndrome (unco)
Juberg Marsidi Genetic syndrome (unco)
Marinesco Sjogren syndrome
Myhre Syndrome
Pitt syndrome (4p16.3)
Schilder disease/Adrenoleukodystrophy
Timothy Calcium channel anomaly
Beckwith-Wiedemann Syndrome
MELAS Encephalopathy
Pallister W Syndrome
Pseudohypoparathyroidism
Zellweger Cerebrhepatorenal syndrome
Acrocephalosyndactyly type III syndrome
Apert syndrome
Bartter's syndrome
Bird-headed dwarf of Seckel
Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3)
Canavan disease
Chondrodysplasia punctata/calcificans (Conradi)
Cockayne syndrome
Cryptophthalmos (Fraser) syndrome
Dysautonomia, familial
Hallervorden-Spatz disease (PKAN/NBIA)
Hermann's syndrome
Hypothalamic hypogonadism, Kallman's
Incontinentia pigmenti/hereditary
Kearns-Sayre Ophthalmoplegic Syndrome
Laurence-Moon-Biedel syndrome
Leprechaunism
Leukodystrophy, Krabbe
Lipodystrophy, generalized
Menkes steely hair disease
Myotonia atrophica (Steinert's disease)
Oculocerebrorenal dystrophy/Lowe syndrome
Pelizaeus-Merzbacher disease
Schwartz-Jampel syndrome
Scott's Craniodigital syndrome
Sjogren-Larsson syndrome
Smith-Lemli-Opitz syndrome
Sneddon/Livedo reticularis syndrome
Stickler syndrome
Treacher Collins syndrome
Von Hipple-Lindau disease/Retinocerebellar angiomas
Williams syndrome/Elfin facies
Wyburn-Mason syndrome
18p chromosome deletion complex
Abducted thumbs syndrome
Acrocallosal syndrome (ACS)
Adducted thumbs-Mental retardation syndrome
Andermann Syndrome
Brooks syndrome
Cerebellar ataxia/Cayman type
Cerebrocostomandibular CCM Syndrome
Chromosome 20 deletion/Ring syndrome
Chudley Syndrome 1
Congenital Muscular Dystrophy
Cowden disease/CD (10q23.31)
Craniofrontonasal Syndrome (CFNS)
Cryopyrin-associated Periodic Syndrome (CAPS)
Curran acrorenal syndrome
Faciocardiorenal Syndrome (Eastman-Bixler)
Hereditary autonomic/Sensory neuropathy (HSN III)
Kabuki make-up syndrome
MASA Syndrome
Michelin tire baby syndrome
Netherton's Syndrome
Odontoonychodermal dysplasia (Fadhill)
Orocraniodigital (Juberg-Hayward) Syndrome
Reiger Syndrome
Rosenberg-Bergstrom Syndrome
Say Syndrome 1
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