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Results 1 - 10 of 582 for De
  1. Koolen-de Vries syndrome 
    Koolen-de Vries syndrome is a disorder characterized by developmental delay and mild to moderate intellectual disability. People with this disorder typically ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
  2. Mal de Meleda 
    Mal de Meleda is a rare skin disorder that begins in early infancy. Affected individuals have a condition known as palmoplantar keratoderma, in which the ...
    https://medlineplus.gov/genetics/condition/mal-de-meleda - Genetics
  3. Cornelia de Lange syndrome 
    Cornelia de Lange syndrome is a developmental disorder that affects many parts of the body. The features of this ... and range from relatively mild to severe.Cornelia de Lange syndrome is characterized by slow growth before ...
    https://medlineplus.gov/.../condition/cornelia-de-lange-syndrome - Genetics
  4. Tourette syndrome 
    ... gene. Chronic motor and vocal tic disorder Gilles de la Tourette syndrome Gilles de la Tourette's syndrome GTS TD Tourette disorder ... Organization for Rare Disorders (NORD) ClinicalTrials.gov GILLES DE LA TOURETTE SYNDROME; GTS PubMed Abelson JF, Kwan ...
    https://medlineplus.gov/genetics/condition/tourette-syndrome - Genetics
  5. Atelosteogenesis type 2 
    ... signs and symptoms of the condition. AO2 Atelosteogenesis de la Chapelle type Atelosteogenesis, type 2 De la Chapelle dysplasia McAlister dysplasia Neonatal osseous dysplasia ...
    https://medlineplus.gov/genetics/condition/atelosteogenesis-type-2 - Genetics
  6. Septo-optic dysplasia 
    ... each cell is sufficient to cause the condition. De Morsier syndrome Septooptic dysplasia SOD Genetic Testing Registry: ... Epub 2008 Feb 6. Citation on PubMed McNay DE, Turton JP, Kelberman D, Woods KS, Brauner R, ...
    https://medlineplus.gov/genetics/condition/septo-optic-dysplasia - Genetics
  7. Spinocerebellar ataxia type 36 
    ... from two regions: western Japan and the Costa de Morte in Galicia, Spain. SCA36 is caused by ... down from the affected father. Asidan ataxia Costa de Morte ataxia SCA36 Spinocerebellar ataxia 36 Genetic Testing ...
    https://medlineplus.gov/.../condition/spinocerebellar-ataxia-type-36 - Genetics
  8. VLDLR-associated cerebellar hypoplasia 
    ... without quadrupedal locomotion Cerebellar hypoplasia, VLDLR-associated CHMRQ1 DES-VLDLR Dysequilibrium syndrome-VLDLR VLDLR-CH VLDLRCH Genetic ...
    https://medlineplus.gov/.../vldlr-associated-cerebellar-hypoplasia - Genetics
  9. Caffey disease 
    ... the disorder in their family. Caffey-Silverman syndrome De Toni-Caffey disease Infantile cortical hyperostosis Genetic Testing ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  10. Adenylosuccinate lyase deficiency 
    Adenylosuccinate lyase deficiency is a neurological disorder that causes brain dysfunction (encephalopathy) leading to delayed development of mental and movement abilities ( ...
    https://medlineplus.gov/.../adenylosuccinate-lyase-deficiency - Genetics
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