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TBC1D24
- Doors Syndrome
- Door Syndrome
ASL
- Argininosuccinic Aciduria
PMM2
- Pmm2 Deficiency
CAV3
- Rippling Muscle Disease 1
ACO2
- Infantile Cerebellar-Retinal Degeneration
SRPX2
- Rolandic Epilepsy, Mental Retardation, And Speech Dyspraxia, X-Linked
TH
- Delirium Tremens
- Tyrosine Hydroxylase Deficiency
NALCN
- Hypotonia-Speech Impairment-Severe Cognitive Delay Syndrome
ATP6V1B2
- Autosomal Dominant Deafness-Onychodystrophy Syndrome
IDH2
- Oligodendroglioma
PLCB1
- Oligodendroglioma
- Early Infantile Epileptic Encephalopathy 12
TBX22
- Congenital Radioulnar Synostosis
IDH1
- Oligodendroglioma
MED12
- Phyllodes Tumor
AP3D1
- Albinism
TYR
- Albinism
SMAD6
- Congenital Radioulnar Synostosis
MITF
- Albinism
CLOCK
- Delirium Tremens
GRM8
- Delirium Tremens