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Asperger syndrome -
Gilles de laTourette disorder -
Color blindness -
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Phenylketonuria -
Hemochromatosis -
Alopecia -
Albinism
All items (122)
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Adrenogenital syndrome
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Adrenoleukodystrophy
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Albinism
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Alexander disease
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Alopecia
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Alternating hemiplegia of childhood
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Amaurotic familial idiocy
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Androgenetic alopecia
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Aneuploidy
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Angelman syndrome
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Asperger syndrome
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Category:Autosomal dominant disorders
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Autosomal dominant nocturnal frontal lobe epilepsy
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Category:Autosomal trisomies
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Category:Autosome disorders
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Canavan disease
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Charcot-Marie-Tooth disease
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Childhood absence epilepsy
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Chromosomal abnormalities
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Chromosome 15q partial deletion
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Chromosome disorders
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Category:Chromosome disorders
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Ciliopathies
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Coffin-Lowry syndrome
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Cohen syndrome
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Color blindness
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Congenital adrenal hyperplasia
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Category:Congenital disorders
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Category:Congenital genetic disorders
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Cornelia de Lange Syndrome
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Crohn's disease
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Cystic fibrosis
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G
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Gaucher's disease
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Category:Genes associated with intellectual disabilities
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Genetic disorders
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Category:Genetic disorders associated with intellectual disabilities
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Category:Genetic disorders associated with seizures
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Category:Genetic disorders with OMIM but no gene
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Gilles de laTourette disorder
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Gulf War syndrome
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M
S
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Sandhoff disease
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Category:Sex chromosome disorders
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Category:Sex linked hereditary disorders
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Sex linked hereditary disorders
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Sickle cell disease
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Smith-Magenis syndrome
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Sotos syndrome
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Spinal muscular atrophies
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Spinal muscular atrophy
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Spinal muscular atrophy with progressive myoclonic epilepsy
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Spinocerebellar ataxia
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Spinocerebellar ataxias
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