|
gptkb:congenital_hyperinsulinism
|
E16.1
|
|
gptkb:familial_hypocalciuric_hypercalcemia
|
E83.5
|
|
gptkb:Turner_syndrome
|
Q96
|
|
gptkb:ALS
|
G12.2
|
|
gptkb:L90
|
Atrophic disorders of skin
|
|
gptkb:Apert_syndrome
|
Q87.0
|
|
gptkb:M33.0
|
M30-M36 Systemic connective tissue disorders
|
|
gptkb:Parkinson_Disease,_Postencephalitic
|
G21.1
|
|
gptkb:Disorder,_Seizure
|
gptkb:G40
|
|
gptkb:erythromelalgia
|
I73.8
|
|
gptkb:extranodal_marginal_zone_lymphoma
|
C88.4
|
|
gptkb:cerebellar_mutism_syndrome
|
R47.01
|
|
gptkb:M30:_Polyarteritis_nodosa_and_related_conditions
|
M30-M36: Systemic connective tissue disorders
|
|
gptkb:D98
|
Other specified chromosomal abnormalities, not elsewhere classified
|
|
gptkb:hATTR_amyloidosis
|
E85.1
|
|
gptkb:clear_cell_renal_carcinoma
|
gptkb:C64
|
|
gptkb:autoimmune_lymphoproliferative_syndrome_(ALPS)
|
D47.Z2
|
|
gptkb:Night_Terrors
|
F51.4
|
|
gptkb:leukemia
|
gptkb:C91.0
|
|
gptkb:pulmonary_aspergillosis
|
B44.0
|