Phosphoglucomutase 3-related congenital disorder of glycosylation 1187623009
SNOMED CT code
SNOMED code | 1187623009 |
---|---|
name | Phosphoglucomutase 3-related congenital disorder of glycosylation |
status | active |
date introduced | 2022-01-31 |
fully specified name(s) | Phosphoglucomutase 3-related congenital disorder of glycosylation (disorder) |
synonyms |
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attributes - group1 | |
Occurrence | Congenital 255399007 |
attributes - group2 | |
Pathological process | Abnormal immune process 769247005 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Inborn error of metabolism 86095007 Disorder of glycoprotein metabolism 238045003 Carbohydrate-deficient glycoprotein syndrome 238049009 Phosphoglucomutase 3-related congenital disorder of glycosylation 1187623009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital immunodeficiency disease 36138009 Phosphoglucomutase 3-related congenital disorder of glycosylation 1187623009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Immunodeficiency disorder 234532001 Primary immune deficiency disorder 58606001 Combined immunodeficiency disease 442459007 Phosphoglucomutase 3-related congenital disorder of glycosylation 1187623009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Phosphoglucomutase 3-related congenital disorder of glycosylation 1187623009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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