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Results 1 - 10 of 39 for FG syndrome
  1. FG syndrome 
    FG syndrome is a genetic condition that affects many parts of the body and occurs almost exclusively in males. "FG" represents the surname initials of the ...
    https://medlineplus.gov/genetics/condition/fg-syndrome - Genetics
  2. MED12 gene 
    ... the MED12 gene have been found to cause FG syndrome, which is characterized by intellectual disability, behavioral problems, ... anal opening (imperforate anus).The mutations that cause FG syndrome each change a single protein building block (amino ...
    https://medlineplus.gov/genetics/gene/med12 - Genetics
  3. Developmental Disabilities (National Library of Medicine)  
    What are developmental disabilities? Developmental disabilities are conditions that are usually present at birth. They can affect a child's growth and ...
    https://medlineplus.gov/developmentaldisabilities.html - Health Topics
  4. FLNA gene 
    ... This Health Condition MedlinePlus Genetics provides information about FG syndrome More About This Health Condition ABP-280 ABPX ...
    https://medlineplus.gov/genetics/gene/flna - Genetics
  5. CASK-related intellectual disability 
    ... Najm type National Organization for Rare Disorders (NORD) FG SYNDROME 4; FGS4 INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  6. CASK gene 
    ... This Health Condition MedlinePlus Genetics provides information about FG syndrome More About This Health Condition calcium/calmodulin-dependent ...
    https://medlineplus.gov/genetics/gene/cask - Genetics
  7. Hyaline fibromatosis syndrome 
    ... Rokicki D, Dal Peraro M, van der Goot FG. In-depth analysis of hyaline fibromatosis syndrome frameshift mutations at the same site reveal the ...
    https://medlineplus.gov/.../condition/hyaline-fibromatosis-syndrome - Genetics
  8. ANTXR2 gene 
    ... Rokicki D, Dal Peraro M, van der Goot FG. In-depth analysis of hyaline fibromatosis syndrome frameshift mutations at the same site reveal the ...
    https://medlineplus.gov/genetics/gene/antxr2 - Genetics
  9. Sheldon-Hall syndrome 
    ... on PubMed Central Toydemir RM, Rutherford A, Whitby FG, Jorde LB, Carey JC, Bamshad MJ. Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome. Nat Genet. 2006 May; ...
    https://medlineplus.gov/genetics/condition/sheldon-hall-syndrome - Genetics
  10. KBG syndrome 
    ... Lo-Castro A, Brancati F, Digilio MC, Garaci FG, Bollero P, Alfieri P, Curatolo P. Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations. Am J Med Genet ...
    https://medlineplus.gov/genetics/condition/kbg-syndrome - Genetics
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