|
gptkb:paraganglioma_syndromes
|
C0349676
|
|
gptkb:Charcot-Marie-Tooth_disease_type_1
|
C0268186
|
|
gptkb:ORPHA:58
|
C0010674
|
|
gptkb:familial_atypical_multiple_mole_melanoma_syndrome
|
C0342417
|
|
gptkb:Medullary_thyroid_carcinoma
|
C0027750
|
|
gptkb:left_bundle_branch
|
C0226002
|
|
gptkb:Diseases_of_the_circulatory_system
|
C0012634
|
|
gptkb:LQT2
|
C1860452
|
|
gptkb:vena_portae_hepatis
|
C0032696
|
|
gptkb:familial_exudative_vitreoretinopathy
|
C0017416
|
|
gptkb:dystrophia_myotonica
|
C0026827
|
|
gptkb:ORPHA:215
|
C0010674
|
|
gptkb:ORPHA:166
|
C0010674
|
|
gptkb:ORPHA:482
|
C1860452
|
|
gptkb:Von_Hippel-Lindau_syndrome
|
C0042790
|
|
gptkb:SCA3
|
C0085437
|
|
gptkb:infraorbital_nerve
|
C0021361
|
|
gptkb:ventral_tegmental_area
|
C0228214
|
|
gptkb:ORPHA792
|
C1860452
|
|
gptkb:Von_Hippel-Lindau_Disease
|
C0042790
|