Hypermethioninemia encephalopathy due to deficiency of adenosine kinase 763721006
SNOMED CT code
SNOMED code | 763721006 |
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name | Hypermethioninemia encephalopathy due to deficiency of adenosine kinase |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder) |
synonyms |
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attributes - group2 | |
Due to | Deficiency of adenosine kinase 124314009 |
attributes - group1 | |
Occurrence | Congenital 255399007 |
Finding site | Brain structure 12738006 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Hypermethioninemia encephalopathy due to deficiency of adenosine kinase 763721006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of organic acid metabolism 116021002 Disorder of amino acid metabolism 44779003 Disorder of amino acid and organic acid metabolism 237911005 Disorder of sulfur-bearing amino acid metabolism 28882002 Hypermethioninemia 43123004 Hypermethioninemia encephalopathy due to deficiency of adenosine kinase 763721006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic encephalopathy 50122000 Hypermethioninemia encephalopathy due to deficiency of adenosine kinase 763721006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Hypermethioninemia encephalopathy due to deficiency of adenosine kinase 763721006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Hypermethioninemia encephalopathy due to deficiency of adenosine kinase 763721006 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Central nervous system complication 87536007 Hypermethioninemia encephalopathy due to deficiency of adenosine kinase 763721006 |
ancestors | sorted most to least specific
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cpt crosswalks |
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