SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Developmental hereditary disorder  363070008

GM1 gangliosidosis  238025006

Infantile GM1 gangliosidosis   238026007

SNOMED CT code


SNOMED code238026007
nameInfantile GM1 gangliosidosis
statusactive
date introduced2002-01-31
fully specified name(s)Infantile GM1 gangliosidosis (disorder)
synonyms
  • Deficiency of beta-galactosidase isoenzymes A, B AND C
  • Infantile GM>1< gangliosidosis
  • GM>1< gangliosidosis, type 1
  • Infantile gangliosidosis with bony involvement
  • Generalised gangliosidosis
  • Infantile GM1 gangliosidosis
  • Generalized gangliosidosis
attributes - group1
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Associated morphologyDysplasia   25723000
Finding siteBone structure   272673000
attributes - group2
OccurrenceCongenital   255399007
Finding siteNervous system structure   25087005
parentsGM1 gangliosidosis   238025006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          GM1 gangliosidosis   238025006
            Infantile GM1 gangliosidosis   238026007

ancestors
sorted most to least specific
cpt crosswalks

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