|
gptkb:CMD_with_laminin_alpha_2_deficiency
|
rare
|
|
gptkb:Haden's_Syndrome
|
rare condition
|
|
gptkb:Vascular_Ehlers-Danlos_syndrome
|
rare disorder
|
|
gptkb:Cowden_syndrome
|
1 in 200,000
|
|
gptkb:impetigo
|
high in developing countries
|
|
gptkb:Late-onset_Alzheimer's_Disease
|
most common form of dementia
|
|
gptkb:cyanotic_heart_disease
|
1 in 100 to 1 in 200 live births
|
|
gptkb:Glycogen_storage_disease
|
rare
|
|
gptkb:Churg-Strauss_syndrome
|
rare
|
|
gptkb:cytomegalovirus
|
common worldwide
|
|
gptkb:late-onset_Pompe_disease
|
rare disease
|
|
gptkb:Anderson-Fabry_disease
|
1 in 100,000 females
|
|
gptkb:Canis_lupus
|
more common in women
|
|
gptkb:sickle_cell_disease
|
more common in Mediterranean descent
|
|
gptkb:pheochromocytomas
|
rare
|
|
gptkb:X-linked_immunodeficiency
|
1 in 100,000 male births
|
|
gptkb:Attention_Deficit_Hyperactivity_Disorder_(ADHD)
|
5% of children
|
|
gptkb:Ehlers-Danlos_syndrome
|
1 in 5,000 to 1 in 20,000
|
|
gptkb:LGMD2_F
|
rare disorder
|
|
gptkb:Ataxia-telangiectasia
|
rare disorder
|