Update Neurologic Underlying Medical Condition Refset

Description

Add these concepts to Neurologic Underlying Medical Condition Refset

SNOMED ID

SNOMED FSN

281004

Dementia associated with alcoholism (disorder)

26929004

Alzheimer's disease (disorder)

230724001

Cerebral amyloid angiopathy (disorder)

390936003

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)

792004

Jakob-Creutzfeldt disease (disorder)

230270009

Frontotemporal dementia (disorder)

312991009

Senile dementia of the Lewy body type (disorder)

56267009

Multi-infarct dementia (disorder)

429998004

Vascular dementia (disorder)

23560001

Asperger's disorder (disorder)

35253001

Attention deficit hyperactivity disorder, predominantly inattentive type (disorder)

406506008

Attention deficit hyperactivity disorder (disorder)

408856003

Autistic disorder (disorder)

613003

Fragile X syndrome (disorder)

110359009

Intellectual disability (disorder)

47437004

Mental handicap (finding)

35919005

Pervasive developmental disorder (disorder)

47311000119103

Static encephalopathy (disorder)

51500006

Complete trisomy 18 syndrome (disorder)

41040004

Complete trisomy 21 syndrome (disorder)

84757009

Epilepsy (disorder)

91175000

Seizure (finding)

41497008

Febrile convulsion (finding)

67434000

Cytochrome-c oxidase deficiency (disorder)

10394003

Friedreich's ataxia (disorder)

25792000

Kearns-Sayre syndrome (disorder)

237995002

Depletion of mitochondrial deoxyribonucleic acid (disorder)

39925003

Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)

718214007

Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)

230426003

Myoclonic epilepsy with ragged red fibers (disorder)

237985009

Pearson's syndrome (disorder)

5335002

Phosphoenolpyruvate carboxykinase deficiency (disorder)

87694001

Pyruvate carboxylase deficiency (disorder)

46683007

Pyruvate dehydrogenase complex deficiency (disorder)

124165006

Deficiency of succinate dehydrogenase (disorder)

387732009

Becker muscular dystrophy (disorder)

111501005

Congenital hereditary muscular dystrophy (disorder)

76670001

Duchenne muscular dystrophy (disorder)

111508004

Emery-Dreifuss muscular dystrophy (disorder)

399091004

Facioscapulohumeral muscular dystrophy (disorder)

240046001

Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)

77956009

Steinert myotonic dystrophy syndrome (disorder)

89369001

Anencephalus (disorder)

32219008

Craniorachischisis (disorder)

55999004

Encephalocele (disorder)

2438005

Iniencephaly (disorder)

414667000

Meningomyelocele (disorder)

67531005

Spina bifida (disorder)

230572002

Neuropathy due to diabetes mellitus (disorder)

302226006

Peripheral nerve disease (disorder)

49049000

Parkinson's disease (disorder)

44695005

Paralysis (finding)

11538006

Quadriplegia (disorder)

405773007

Kyphoscoliosis deformity of spine (disorder)

Assignee

Susan Matney

Reporter

Susan Castillo

Labels

None

Concept ID

None

Concept Name

None

Release Version History

Logica SNOMED Extension July 30 - Q3 2020

Priority

Major
Configure