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Results 1 - 10 of 117 for pass syndrome
  1. McLeod neuroacanthocytosis syndrome 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. McLeod syndrome Genetic Testing Registry: McLeod neuroacanthocytosis syndrome McLeod neuroacanthocytosis ...
    https://medlineplus.gov/.../mcleod-neuroacanthocytosis-syndrome - Genetics
  2. Deafness-dystonia-optic neuronopathy syndrome 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. Deafness syndrome, progressive, with blindness, dystonia, fractures, and mental deficiency ...
    https://medlineplus.gov/...ness-dystonia-optic-neuronopathy-syndrome - Genetics
  3. Otopalatodigital syndrome type 2 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. Cranioorodigital syndrome Faciopalatoosseous syndrome FPO OPD syndrome, type 2 Oto- ...
    https://medlineplus.gov/.../otopalatodigital-syndrome-type-2 - Genetics
  4. Monoamine oxidase A deficiency 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. Brunner syndrome Deficiency of monoamine oxidase A X-linked monoamine ...
    https://medlineplus.gov/.../condition/monoamine-oxidase-a-deficiency - Genetics
  5. Mucopolysaccharidosis type II 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. Hunter syndrome I2S deficiency Iduronate 2-sulfatase deficiency MPS II ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-ii - Genetics
  6. Otopalatodigital syndrome type 1 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. Cranioorodigital syndrome Faciopalatoosseous syndrome FPO OPD syndrome, type 1 Oto- ...
    https://medlineplus.gov/.../otopalatodigital-syndrome-type-1 - Genetics
  7. Leigh syndrome 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons. Occasionally, Leigh syndrome is caused by genetic variants that occur spontaneously, ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  8. Primary coenzyme Q10 deficiency 
    ... function, which allows protein from the blood to pass into the urine (proteinuria). Other signs and symptoms of nephrotic syndrome include increased cholesterol in the blood (hypercholesterolemia), an ...
    https://medlineplus.gov/.../primary-coenzyme-q10-deficiency - Genetics
  9. Timothy syndrome 
    ... for an affected individual to be able to pass on the disease-causing variant. Although rare, some people with Timothy syndrome inherit the altered gene from an unaffected parent ...
    https://medlineplus.gov/genetics/condition/timothy-syndrome - Genetics
  10. Opitz G/BBB syndrome 
    ... of X-linked inheritance is that fathers cannot pass X-linked traits to their sons.Rarely, Opitz G/BBB syndrome is inherited in an autosomal dominant pattern, which ...
    https://medlineplus.gov/genetics/condition/opitz-g-bbb-syndrome - Genetics
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