Genetic Diseases & Conditions - Mental health and behaviour

Altered genes or chromosomes may lead to conditions that impair a person's ability to think, remember, learn, or react to other people and the environment.

AD see Alzheimer disease
Adrenoleukodystrophy see X-linked adrenoleukodystrophy
Adrenomyeloneuropathy see X-linked adrenoleukodystrophy
Alzheimer disease
Angelman syndrome
AS see Angelman syndrome
Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome see Rett syndrome
BDLS see Cornelia de Lange syndrome
Beuren syndrome see Williams syndrome
Brachmann-De Lange Syndrome see Cornelia de Lange syndrome
CADASIL
CDLS see Cornelia de Lange syndrome
Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy see CADASIL
Cerebral autosomal dominant ateriopathy with subcortical infarcts and leukoencephalopathy see CADASIL
Cerebroatrophic Hyperammonemia see Rett syndrome
Choreoathetosis self-mutilation syndrome see Lesch-Nyhan syndrome
chromosome 17p deletion syndrome see Smith-Magenis syndrome
Chronic Motor and Vocal Tic Disorder see Tourette syndrome
Complete HPRT deficiency see Lesch-Nyhan syndrome
Complete hypoxanthine-guanine phosphoribosyltransferase deficiency see Lesch-Nyhan syndrome
Cornelia de Lange syndrome
Costello syndrome
DAT - Dementia Alzheimer's type see Alzheimer disease
De Lange Syndrome see Cornelia de Lange syndrome
7-Dehydrocholesterol reductase deficiency see Smith-Lemli-Opitz syndrome
deletion 17p syndrome see Smith-Magenis syndrome
Down syndrome
Elfin Facies Syndrome see Williams syndrome
Elfin facies with hypercalcemia see Williams syndrome
faciocutaneoskeletal syndrome see Costello syndrome
familial Alzheimer disease (FAD) see Alzheimer disease
familial Turner syndrome see Noonan syndrome
Familial vascular leukoencephalopathy see CADASIL
FCS syndrome see Costello syndrome
Female Pseudo-Turner Syndrome see Noonan syndrome
fra(X) syndrome see fragile X syndrome
fragile X syndrome
FRAXA Syndrome see fragile X syndrome
FXS see fragile X syndrome
Gilles de la Tourette Syndrome see Tourette syndrome
HPRT - Hypoxanthine-guanine phosphoribosyltransferase deficiency see Lesch-Nyhan syndrome
Huntington disease
Hypercalcemia-Supravalvar Aortic Stenosis see Williams syndrome
hypoxanthine phosphoribosyltransferse (HPRT) deficiency see Lesch-Nyhan syndrome
Infantile hypercalcemia see Williams syndrome
Inherited Human Transmissible Spongiform Encephalopathies see prion disease
Juvenile gout, choreoathetosis, mental retardation syndrome see Lesch-Nyhan syndrome
juvenile hyperuricemia syndrome see Lesch-Nyhan syndrome
Lacunar Dementias see CADASIL
Late Onset Alzheimer Disease see Alzheimer disease, type 2
Late-Onset Familial Alzheimer Disease (AD2) see Alzheimer disease, type 2
Lesch-Nyhan syndrome
LNS see Lesch-Nyhan syndrome
Male Turner Syndrome see Noonan syndrome
Marker X syndrome see fragile X syndrome
Martin-Bell Syndrome see fragile X syndrome
Multi-Infarct Dementia see CADASIL
Noonan syndrome
Prader-Labhart-Willi syndrome see Prader-Willi syndrome
Prader-Willi syndrome
Presenile and senile dementia see Alzheimer disease
primary hyperuricemia syndrome see Lesch-Nyhan syndrome
Primary Senile Degenerative Dementia see Alzheimer disease
prion disease
Progressive Chorea, Chronic Hereditary (Huntington) see Huntington disease
pseudo-Ullrich-Turner syndrome see Noonan syndrome
PWS see Prader-Willi syndrome
Rett syndrome
RSH Syndrome see Smith-Lemli-Opitz syndrome
RTS see Rett syndrome
RTT see Rett syndrome
Schilder-Addison Complex see X-linked adrenoleukodystrophy
SDAT see Alzheimer disease
Senile Dementia see Alzheimer disease, type 2
SLO syndrome see Smith-Lemli-Opitz syndrome
SLOS see Smith-Lemli-Opitz syndrome
Smith-Lemli-Opitz syndrome
Smith-Magenis syndrome
SMS see Smith-Magenis syndrome
Supravalvar aortic stenosis syndrome see Williams syndrome
17p- syndrome see Smith-Magenis syndrome
Total HPRT deficiency see Lesch-Nyhan syndrome
Total hypoxanthine-guanine phosphoribosyl transferase deficiency see Lesch-Nyhan syndrome
Tourette syndrome
Transmissible Dementias see prion disease
Transmissible Spongiform Encephalopathies see prion disease
triple X syndrome
Triplo X syndrome see triple X syndrome
Trisomy 21 see Down syndrome
Trisomy X see triple X syndrome
TSEs see prion disease
Turner-like syndrome see Noonan syndrome
Turner syndrome in female with X chromosome see Noonan syndrome
Turner's phenotype, karyotype normal see Noonan syndrome
Ullrich-Noonan syndrome see Noonan syndrome
WBS see Williams syndrome
Williams syndrome
WMS see Williams syndrome
WS see Williams syndrome
X-linked adrenoleukodystrophy
X-linked hyperuricemia see Lesch-Nyhan syndrome
X-linked mental retardation and macroorchidism see fragile X syndrome
X-linked primary hyperuricemia see Lesch-Nyhan syndrome
X-linked uric aciduria enzyme defect see Lesch-Nyhan syndrome
47,XX,+21 see Down syndrome
47,XXX see triple X syndrome
XXX syndrome see triple X syndrome
47,XY,+21 see Down syndrome
47,XYY syndrome
XYY Karyotype see 47,XYY syndrome
XYY syndrome see 47,XYY syndrome
YY syndrome see 47,XYY syndrome

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