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Genetic / Hereditary

This dimension names the agent that actually causes a medical condition, a pathogen, a genetic mutation or an environmental factor. Wikipedia notes that "a disease may be caused by external factors such as pathogens or by internal dysfunctions." Browsing this way collects every condition caused by the same agent.

Facts

Comparison

ICD-10 Chapter Number

VI 1

ICD-10 Code Range

G00-G99 1

Genetic / Hereditary

88 entries

Body System

ICD-10 Chapter

Communicable or Non-communicable

Transmission Route

Era (First Described)

Treated By

Discoverer

ALS

Alternating hemiplegia of childhood

Amyotrophic Lateral Sclerosis

Ataxia with oculomotor apraxia type 1

Attention Deficit Hyperactivity Disorder

Autism

Autosomal dominant leukodystrophy with autonomic disease

Behr syndrome

Bethlem myopathy

Biotin-thiamine-responsive basal ganglia disease

Central core disease

Centronuclear myopathy

Cerebral folate deficiency

Cerebroretinal microangiopathy with calcifications and cysts

Charcot-Marie-Tooth Disease

Childhood dementia

Chorea-acanthocytosis

Christianson syndrome

Cobb syndrome

Congenital Insensitivity to Pain

Congenital insensitivity to pain with anhidrosis

Congenital myasthenic syndrome

Cramp Fasciculation Syndrome

Dejerine-Sottas disease

Dentatorubral-pallidoluysian atrophy

Distal myopathy

Dopamine-responsive dystonia

Dravet syndrome

Duchenne muscular dystrophy

Epilepsy-intellectual disability in females

Familial amyloid polyneuropathy

Familial dysautonomia

Familial hemiplegic migraine

Friedreich's Ataxia

Generalized epilepsy with febrile seizures plus

Gerstmann-Sträussler-Scheinker syndrome

Hereditary neuralgic amyotrophy

Hereditary sensory and autonomic neuropathy type I

Hereditary spastic paraplegia

HNRNPH2-related disorders

Huntington's Disease

Hyperekplexia

Hyperkalemic periodic paralysis

Hypokalemic periodic paralysis

Infantile neuroaxonal dystrophy

Jansky-Bielschowsky disease

Jordan's syndrome

Juvenile myoclonic epilepsy

Kufor-Rakeb syndrome

Lafora disease