SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Congenital malformation  276654001

Congenital anomaly of the hematopoietic system  40888008

HNSHA due to aldolase A deficiency   111578003

SNOMED CT code


SNOMED code111578003
nameHNSHA due to aldolase A deficiency
statusremoved
date introduced2002-01-31
fully specified name(s)Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency (disorder)
synonyms
  • HNSHA due to aldolase A deficiency
  • Fructose 1,6-biphosphate aldolase A deficiency
  • Aldolase A deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to aldolase A deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to aldolase A deficiency
  • Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to aldolase A deficiency
parentsCongenital anomaly of the hematopoietic system   40888008
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital anomaly of the hematopoietic system   40888008
            HNSHA due to aldolase A deficiency   111578003  removed: 2022-01-31

ancestors
sorted most to least specific
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