UBE2S - ubiquitin conjugating enzyme E2 S Gene

Chromosome 5q14.3 Deletion Syndrome

5q14.3 Microdeletion Syndrome

Mental Retardation, Autosomal Dominant 20

NEDHSIL

Autosomal Dominant Mental Retardation 20

Mrd20

Del(5)(Q14.3)

Monosomy 5q14.3

Intellectual Disability, Autosomal Dominant 20

Mental Retardation, Autosomal Dominant 20, Formerly

Mrd20, Formerly

Mental Retardation, Stereotypic Movements, Epilepsy, And/Or Cerebral Malformations

5q14.3 Deletion Syndrome

Autosomal Dominant Intellectual Disability 20

Mental Retardation, Autosomal Dominant, Type 20

Liddle Syndrome

Pseudoaldosteronism

Liddle'S Syndrome

LIDLS1

Lidls

Pseudohyperaldosteronism

Pseudoprimary Hyperaldosteronism

Pseudohyperaldosteronism Type 1

Liddles Syndrome

Juvenile-Onset Parkinson Disease

Hypophosphatemic Nephrolithiasis/Osteoporosis 1

NPHLOP1

Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1

Nephrolithiasis/Osteoporosis, Hypophosphatemic, Type 1

Complex Cortical Dysplasia With Other Brain Malformations 6

CDCBM6

Cdcbm56

Dysplasia ,Cortical, Complex, With Other Brain Malformations, Type 6

Parkinson Disease

Parkinson'S Disease

PD

PARK

Parkinson Disease, Susceptibility To

Late Onset Parkinson'S Disease

Late Onset Parkinson Disease

Paralysis Agitans

Primary Parkinsonism

Idiopathic Parkinson Disease

Parkinson'S

Parkinson Disease, Late-Onset, Susceptibility To

Parkinson Disease, Age Of Onset, Modifier

Lewy Body Parkinson Disease

Idiopathic Parkinson'S Disease

Pd - [Parkinson Disease]

Parkinson Disease Nos

Parkinson, Nos

Primary Parkinson Disease