|
gptkb:NF1_gene
|
50% for offspring of affected individual
|
|
gptkb:CMTX
|
males more severely affected
|
|
gptkb:SCA1
|
50% if one parent affected
|
|
gptkb:myotonic_dystrophy_type_2
|
50% for offspring of affected parent
|
|
gptkb:spinocerebellar_ataxia_type_3
|
50% if one parent affected
|
|
gptkb:Ataxia-telangiectasia
|
25% if both parents are carriers
|
|
gptkb:Maturity_Onset_Diabetes_of_the_Young_type_2_(MODY2)
|
50% for offspring if one parent is affected
|
|
gptkb:SCA3
|
50% for offspring of affected parent
|
|
gptkb:beta-thalassemia_minor
|
25% chance of major if both parents have minor
|
|
gptkb:CMTX
|
females may be carriers
|
|
gptkb:Huntington's_disease
|
50% if one parent affected
|