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Results 1 - 10 of 443 for Van
  1. Ellis-van Creveld syndrome 
    Ellis-van Creveld syndrome is an inherited disorder of bone growth that results in very short stature (dwarfism). People with this condition have particularly ...
    https://medlineplus.gov/.../condition/ellis-van-creveld-syndrome - Genetics
  2. Van der Woude syndrome 
    Van der Woude syndrome is a condition that affects the development of the face. Many people with ...
    https://medlineplus.gov/genetics/condition/van-der-woude-syndrome - Genetics
  3. SOST-related sclerosing bone dysplasia 
    ... of SOST-related sclerosing bone dysplasia: sclerosteosis and van Buchem disease. The two forms are distinguished by ... sclerosteosis may also have absent or malformed nails.Van Buchem disease represents the milder form of the ...
    https://medlineplus.gov/.../sost-related-sclerosing-bone-dysplasia - Genetics
  4. Riboflavin transporter deficiency neuronopathy 
    ... that were once considered distinct disorders: Brown-Vialetto-Van Laere syndrome (BVVLS) and Fazio-Londe disease. The ... signs and symptoms of the condition. Brown-Vialetto-Van Laere syndrome BVVLS Fazio-Londe disease Fazio-Londe ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  5. 7q11.23 duplication syndrome 
    ... 23 duplication syndrome Dup(7)(q11.23) Somerville-Van der Aa syndrome Trisomy 7q11.23 WBS duplication ... on PubMed or Free article on PubMed Central Van der Aa N, Rooms L, Vandeweyer G, van ...
    https://medlineplus.gov/.../condition/7q1123-duplication-syndrome - Genetics
  6. Megalencephalic leukoencephalopathy with subcortical cysts 
    ... Vacuolating leukoencephalopathy Vacuolating megalencephalic leukoencephalopathy with subcortical cysts Van der Knaap disease Genetic Testing Registry: Megalencephalic leukoencephalopathy ...
    https://medlineplus.gov/...eukoencephalopathy-with-subcortical-cysts - Genetics
  7. Focal dermal hypoplasia 
    ... Pauli RM. Probable identity of Goltz syndrome and Van Allen-Myhre syndrome: evidence from phenotypic evolution. Am ... Celli J, Lampe A, Gabbett MT, Ousager LB, van der Smagt JJ, Soller M, Stattin EL, Mannens ...
    https://medlineplus.gov/genetics/condition/focal-dermal-hypoplasia - Genetics
  8. Cerebrotendinous xanthomatosis 
    ... cholesterinosis Cerebrotendinous cholesterinosis Cholestanol storage disease Cholestanolosis CTX Van Bogaert-Scherer-Epstein disease Genetic Testing Registry: Cholestanol ...
    https://medlineplus.gov/.../condition/cerebrotendinous-xanthomatosis - Genetics
  9. Osteogenesis imperfecta 
    Osteogenesis imperfecta (OI) is a group of genetic disorders that mainly affect the bones. The term "osteogenesis imperfecta" means imperfect bone formation. People ...
    https://medlineplus.gov/genetics/condition/osteogenesis-imperfecta - Genetics
  10. Loeys-Dietz syndrome 
    ... E, Morisaki H, Verhagen JMA, de Graaf BM, van de Beek G, Gallo E, Kruithof BPT, Venselaar ... Myers LA, Laga S, Doyle AJ, Oswald G, van Cappellen GWA, Yamanaka I, van der Helm RM, ...
    https://medlineplus.gov/genetics/condition/loeys-dietz-syndrome - Genetics
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