|
gptkb:fascioliasis
|
B66.3
|
|
gptkb:Glycogen_Storage_Disease_Type_I
|
E74.0
|
|
gptkb:Odynophagia
|
R13.12
|
|
gptkb:myasthenia_gravis
|
G70.0
|
|
gptkb:Obstructive_Liver_Disease
|
K83.1
|
|
gptkb:homocystinuria
|
E72.1
|
|
gptkb:Guillain–Barré_syndrome
|
G61.0
|
|
gptkb:Rheumatoid_Arthritis
|
gptkb:M06
|
|
gptkb:Lesch-Nyhan_disease
|
E79.1
|
|
gptkb:ameloblastoma
|
D16.0
|
|
gptkb:piebaldism
|
Q80.3
|
|
gptkb:F84.3_Other_childhood_disintegrative_disorder
|
F80-F89 Pervasive developmental disorders
|
|
gptkb:Parkinson's_Disease
|
gptkb:G20
|
|
gptkb:Horner's_syndrome
|
G90.8
|
|
gptkb:small_lymphocytic_lymphoma
|
gptkb:C83.0
|
|
gptkb:CMV
|
B25
|
|
gptkb:Richter's_syndrome
|
C91.1
|
|
gptkb:idiopathic_Parkinsonism
|
gptkb:G20
|
|
gptkb:Hirschsprung_disease
|
Q43.1
|
|
gptkb:roseola_infantum
|
B08.2
|