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Results 1 - 10 of 1,628 for H syndrome
  1. Ornithine translocase deficiency 
    ... hyperammonemia-homocitrullinemia syndrome Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Triple H syndrome Genetic Testing Registry: Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome Hyperornithinemia- ...
    https://medlineplus.gov/.../ornithine-translocase-deficiency - Genetics
  2. Histiocytosis-lymphadenopathy plus syndrome 
    ... of the body. This group of disorders includes H syndrome, pigmented hypertrichosis with insulin-dependent diabetes mellitus (PHID), ... additional signs and symptoms. A characteristic feature of H syndrome is abnormal patches of skin (lesions), typically on ...
    https://medlineplus.gov/...stiocytosis-lymphadenopathy-plus-syndrome - Genetics
  3. Mucopolysaccharidosis type I 
    ... syndrome) MPS III (Sanfilippo syndrome) MPS IV (Morquio syndrome)
    https://medlineplus.gov/ency/article/001204.htm - Medical Encyclopedia
  4. Vici syndrome 
    ... Dionisi-Vici C, Smith L, Gautel M, Jungbluth H. Vici syndrome: a review. Orphanet J Rare Dis. 2016 Feb ... G, Chen Y, Feng D, Hu J, Zhang H. The Vici Syndrome Protein EPG5 Is a Rab7 Effector that Determines ...
    https://medlineplus.gov/genetics/condition/vici-syndrome - Genetics
  5. Majeed syndrome 
    ... article on PubMed Central Ferguson PJ, El-Shanti H. Majeed Syndrome: A Review of the Clinical, Genetic and Immunologic ... PubMed Majeed HA, Al-Tarawna M, El-Shanti H, Kamel B, Al-Khalaileh F. The syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic ...
    https://medlineplus.gov/genetics/condition/majeed-syndrome - Genetics
  6. Mucopolysaccharidosis type I 
    ... into three separate syndromes: Hurler syndrome (MPS I-H), Hurler-Scheie syndrome (MPS I-H/S), and Scheie syndrome (MPS I-S), listed from most to least ... deficiency MPS I MPS I H MPS I H-S MPS I S Mucopolysaccharidosis I Scheie syndrome ... Genetic Testing Registry: Mucopolysaccharidosis type 1 Mucopolysaccharidosis type ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-i - Genetics
  7. Roberts syndrome 
    ... C, Ozono K, Jabs EW, Inui K, Joenje H. Roberts syndrome is caused by mutations in ESCO2, a human ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  8. ESCO2 gene 
    ... C, Ozono K, Jabs EW, Inui K, Joenje H. Roberts syndrome is caused by mutations in ESCO2, a human ...
    https://medlineplus.gov/genetics/gene/esco2 - Genetics
  9. LPIN2 gene 
    ... article on PubMed Central Ferguson PJ, El-Shanti H. Majeed Syndrome: A Review of the Clinical, Genetic and Immunologic ...
    https://medlineplus.gov/genetics/gene/lpin2 - Genetics
  10. Arts syndrome 
    ... Donald JA, Wevers RA, Christodoulou J, van Bokhoven H. Arts syndrome is caused by loss-of-function mutations in ... nih.gov/books/NBK2591/ Citation on PubMed Kremer H, Hamel BC, van ... for a syndrome with X-linked mental retardation, ataxia, weakness, hearing ...
    https://medlineplus.gov/genetics/condition/arts-syndrome - Genetics
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