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Results 1 - 10 of 1,313 for -"cardio kinetic"
  1. Familial cold autoinflammatory syndrome type 2 
    Familial cold autoinflammatory syndrome type 2 is a condition that causes episodes of fever, skin rash, and joint pain. These episodes can be triggered by exposure ...
    https://medlineplus.gov/...ial-cold-autoinflammatory-syndrome-type-2 - Genetics
  2. VEXAS syndrome 
    VEXAS syndrome is a disorder involving episodes of fever and abnormal inflammation. VEXAS is an acronym that stands for the technical terms of key descriptors ...
    https://medlineplus.gov/genetics/condition/vexas-syndrome - Genetics
  3. CUL3-related neurodevelopmental disorder 
    CUL3-related neurodevelopmental disorder is a condition that affects neurological and physical development. Children with CUL3-related neurodevelopmental ...
    https://medlineplus.gov/.../cul3-related-neurodevelopmental-disorder - Genetics
  4. Multiple familial trichoepithelioma 
    Multiple familial trichoepithelioma is a condition involving multiple skin tumors that develop from structures associated with the skin (skin appendages), such ...
    https://medlineplus.gov/.../multiple-familial-trichoepithelioma - Genetics
  5. DLG4-related synaptopathy 
    DLG4-related synaptopathy is a condition that affects neurological development. This condition is characterized by delayed development and mild to moderate ...
    https://medlineplus.gov/genetics/condition/dlg4-related-synaptopathy - Genetics
  6. KCNB1 encephalopathy 
    KCNB1 encephalopathy is a condition characterized by abnormal brain function (encephalopathy), recurrent seizures (epilepsy), and developmental delay.Most people ...
    https://medlineplus.gov/genetics/condition/kcnb1-encephalopathy - Genetics
  7. Cryopyrin-associated periodic syndromes 
    Cryopyrin-associated periodic syndromes (CAPS) are a group of conditions that have overlapping signs and symptoms and the same genetic cause. The group includes ...
    https://medlineplus.gov/.../cryopyrin-associated-periodic-syndromes - Genetics
  8. CYLD cutaneous syndrome 
    CYLD cutaneous syndrome is a genetic condition characterized by the growth of multiple noncancerous (benign) skin tumors. These tumors develop from structures ...
    https://medlineplus.gov/genetics/condition/cyld-cutaneous-syndrome - Genetics
  9. SRD5A3-congenital disorder of glycosylation 
    SRD5A3-congenital disorder of glycosylation (SRD5A3-CDG, formerly known as congenital disorder of glycosylation type Iq) is an inherited condition that causes ...
    https://medlineplus.gov/...d5a3-congenital-disorder-of-glycosylation - Genetics
  10. MN1 C-terminal truncation syndrome 
    MN1 C-terminal truncation (MCTT) syndrome is a condition characterized by intellectual disability, developmental delay, distinctive facial features, and brain ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics
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