SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Congenital disease  66091009

Congenital male infertility  236790005

Congenitally impaired spermatogenesis  236799006

Oligosynaptic infertility   236803007

SNOMED CT code


SNOMED code236803007
nameOligosynaptic infertility
statusactive
date introduced2002-01-31
fully specified name(s)Oligosynaptic infertility (disorder)
synonyms
  • Oligochiasmic infertility
  • Oligosynaptic infertility
attributes - group2
InterpretsFertility, function   397594008
attributes - group1
OccurrenceCongenital   255399007
Finding siteMale genital structure   90264002
attributes - group3
Finding siteTestis structure   40689003
parentsCongenitally impaired spermatogenesis   236799006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital male infertility   236790005
          Congenitally impaired spermatogenesis   236799006
            Oligosynaptic infertility   236803007

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

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