SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Genetic disease  782964007

Hereditary disease  32895009

Autosomal hereditary disorder  1899006

Autosomal recessive hereditary disorder  85995004

Multiple mitochondrial dysfunctions syndrome  720827002

Multiple mitochondrial dysfunctions syndrome type 1   1208485009

SNOMED CT code


SNOMED code1208485009
nameMultiple mitochondrial dysfunctions syndrome type 1
statusactive
date introduced2022-03-31
fully specified name(s)Multiple mitochondrial dysfunctions syndrome type 1 (disorder)
synonyms
  • MMDS1 - multiple mitochondrial dysfunctions syndrome type 1
  • Multiple mitochondrial dysfunctions syndrome type 1
  • NFU1 (NFU1 iron-sulfur cluster scaffold) deficiency
attributes - group1
OccurrenceCongenital   255399007
parentsMultiple mitochondrial dysfunctions syndrome   720827002
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Multiple mitochondrial dysfunctions syndrome   720827002
                Multiple mitochondrial dysfunctions syndrome type 1   1208485009

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

demo
request yours today
 subscribe
start today
 newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.