Diseases Associated With Locomotion
Disease |
Autism
|
Nerve Degeneration
|
Epilepsy
|
Dilated Cardiomyopathy
|
Craniofacial Abnormalities
|
Alzheimer's Disease
|
Anoxia
|
Asphyxia Neonatorum
|
Autism Spectrum Disorder
|
Intellectual Disability
|
Language Development Disorders
|
Colorectal Cancer
|
Charcot-Marie-Tooth Disease, Type 1f
|
Charcot-Marie-Tooth Disease, Type 2e
|
Cognitive Impairment
|
Congenital Abnormalities
|
Deafness, Autosomal Recessive 12
|
Developmental Disabilities
|
Diabetes Mellitus
|
Disease Models, Animal
|
Distal Myopathy, Nonaka Type
|
Epilepsy, Rolandic
|
Epilepsy, X-Linked, With Variable Learning Disabilities And Behavior Disorders
|
Facies
|
Fragile X Syndrome
|
Fragile X Tremor Ataxia Syndrome
|
Frontotemporal Dementia
|
Generalized Epilepsy With Febrile Seizures Plus, Type 1
|
Glucose Intolerance
|
Gonadal Dysgenesis
|
Hemiplegic Migraine, Familial Type 2
|
Hidradenitis Suppurativa, Familial
|
Huntington Disease-Like 2
|
Hyperalgesia
|
Hypertension
|
Hypertrophy
|
Inclusion Body Myopathy Autosomal Recessive
|
Landau-Kleffner Syndrome
|
Learning Disorders
|
Manganese Poisoning
|
Maternally Inherited Leigh Syndrome
|
Melanoma
|
Memory Disorders
|
Morphine Dependence
|
Myositis, Inclusion Body
|
Neurodegenerative Diseases
|
Neuropathy Ataxia And Retinitis Pigmentosa
|
Pick Disease Of The Brain
|
Primary Ovarian Insufficiency
|
Primary Ovarian Insufficiency, Fragile X-Associated
|
Schizophrenia
|
Seizures
|
Febrile Seizures
|
N-Acetylneuraminic Acid Storage Disease
|
Speech Disorders
|
Splenomegaly
|
Substance Withdrawal Syndrome
|
Sudden Infant Death
|
Allan-Herndon-Dudley Syndrome
|
Telomeric 22q13 Monosomy Syndrome
|
Alternating Hemiplegia Of Childhood
|
Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Apraxia
|
Alzheimer Disease Type 4
|
Amyloidosis
|
Angelman Syndrome
|
Autoimmune Disease
|
Breast Carcinoma
|
Brugada Syndrome
|
Brugada Syndrome 5
|
Cardiomyopathy, Dilated, 1u
|
Cardiomyopathy, Dilated, 1v
|