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