|
gptkb:Serogroup_X
|
gptkb:Togo
|
|
gptkb:neovascular_(wet)_age-related_macular_degeneration
|
higher in elderly
|
|
gptkb:infantile-onset_spinocerebellar_ataxia
|
rare
|
|
gptkb:Attention-Deficit/Hyperactivity_Disorder
|
adults
|
|
gptkb:urinary_schistosomiasis
|
parts of South America
|
|
gptkb:CD26_(HbE_mutation)
|
high in Southeast Asia
|
|
gptkb:Munchausen_syndrome
|
rare
|
|
gptkb:hemoglobin_E_disease
|
gptkb:Bangladesh
|
|
gptkb:Christmas_disease
|
about 1 in 30,000 male births
|
|
gptkb:Sleep_Apnea–Hypopnea_Syndrome
|
common in adults
|
|
gptkb:familial_adenomatous_polyposis
|
1 in 8,000 to 1 in 10,000 individuals
|
|
gptkb:fragile_X_syndrome
|
1 in 8,000 females
|
|
gptkb:Redhead
|
1-2% of world population
|
|
gptkb:hh_blood_group
|
gptkb:Iran
|
|
gptkb:HTLV-I
|
gptkb:South_America
|
|
gptkb:Neonatal_intrahepatic_cholestasis_caused_by_citrin_deficiency_(NICCD)
|
rare
|
|
gptkb:Adult-onset_Primary_Familial_Brain_Calcification
|
rare
|
|
gptkb:Albarazado
|
gptkb:Central_America
|
|
gptkb:Loeys-Dietz_syndrome_type_1
|
rare
|
|
gptkb:CLN3_disease
|
rare
|