Code
|
Display
|
26929004
|
Alzheimer's disease (disorder) |
86044005
|
Amyotrophic lateral sclerosis (disorder) |
89369001
|
Anencephalus (disorder) |
23560001
|
Asperger's disorder (disorder) |
406506008
|
Attention deficit hyperactivity disorder (disorder) |
35253001
|
Attention deficit hyperactivity disorder, predominantly inattentive type (disorder) |
408856003
|
Autistic disorder (disorder) |
387732009
|
Becker muscular dystrophy (disorder) |
230724001
|
Cerebral amyloid angiopathy (disorder) |
390936003
|
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) |
128188000
|
Cerebral palsy (disorder) |
51500006
|
Complete trisomy 18 syndrome (disorder) |
41040004
|
Complete trisomy 21 syndrome (disorder) |
111501005
|
Congenital hereditary muscular dystrophy (disorder) |
32219008
|
Craniorachischisis (disorder) |
67434000
|
Cytochrome-c oxidase deficiency (disorder) |
124165006
|
Deficiency of succinate dehydrogenase (disorder) |
281004
|
Dementia associated with alcoholism (disorder) |
52448006
|
Dementia (disorder) |
237995002
|
Depletion of mitochondrial deoxyribonucleic acid (disorder) |
248290002
|
Developmental delay (disorder) |
76670001
|
Duchenne muscular dystrophy (disorder) |
111508004
|
Emery-Dreifuss muscular dystrophy (disorder) |
55999004
|
Encephalocele (disorder) |
84757009
|
Epilepsy (disorder) |
399091004
|
Facioscapulohumeral muscular dystrophy (disorder) |
41497008
|
Febrile convulsion (finding) |
613003
|
Fragile X syndrome (disorder) |
10394003
|
Friedreich's ataxia (disorder) |
230270009
|
Frontotemporal dementia (disorder) |
51928006
|
General paresis - neurosyphilis (disorder) |
88611000119100
|
History of traumatic brain injury (situation) |
386806002
|
Impaired cognition (finding) |
2438005
|
Iniencephaly (disorder) |
110359009
|
Intellectual disability (disorder) |
792004
|
Jakob-Creutzfeldt disease (disorder) |
39925003
|
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder) |
25792000
|
Kearns-Sayre syndrome (disorder) |
405773007
|
Kyphoscoliosis deformity of spine (disorder) |
414667000
|
Meningomyelocele (disorder) |
47437004
|
Mental handicap (finding) |
718214007
|
Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder) |
447292006
|
Mitochondrial encephalomyopathy (disorder) |
56267009
|
Multi-infarct dementia (disorder) |
24700007
|
Multiple sclerosis (disorder) |
240046001
|
Muscular dystrophy with predominantly proximal limb girdle distribution (disorder) |
73297009
|
Muscular dystrophy (disorder) |
91637004
|
Myasthenia gravis (disorder) |
230426003
|
Myoclonic epilepsy with ragged red fibers (disorder) |
253098009
|
Neural tube defect (disorder) |
230572002
|
Neuropathy due to diabetes mellitus (disorder) |
386033004
|
Neuropathy (disorder) |
44695005
|
Paralysis (finding) |
29426003
|
Paralytic syndrome (disorder) |
32798002
|
Parkinsonism (disorder) |
49049000
|
Parkinson's disease (disorder) |
237985009
|
Pearson's syndrome (disorder) |
302226006
|
Peripheral nerve disease (disorder) |
35919005
|
Pervasive developmental disorder (disorder) |
5335002
|
Phosphoenolpyruvate carboxykinase deficiency (disorder) |
87694001
|
Pyruvate carboxylase deficiency (disorder) |
46683007
|
Pyruvate dehydrogenase complex deficiency (disorder) |
11538006
|
Quadriplegia (disorder) |
298382003
|
Scoliosis deformity of spine (disorder) |
91175000
|
Seizure (finding) |
128613002
|
Seizure disorder (disorder) |
312991009
|
Senile dementia of the Lewy body type (disorder) |
67531005
|
Spina bifida (disorder) |
47311000119103
|
Static encephalopathy (disorder) |
77956009
|
Steinert myotonic dystrophy syndrome (disorder) |
127295002
|
Traumatic brain injury (disorder) |
429998004
|
Vascular dementia (disorder) |