SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Congenital malformation  276654001

Congenital malformation syndrome  400038003

Malformation sequence  105989001

Holoprosencephaly sequence   30915001

SNOMED CT code


SNOMED code30915001
nameHoloprosencephaly sequence
statusactive
date introduced2002-01-31
fully specified name(s)Holoprosencephaly sequence (disorder)
synonyms
  • HPE - Holoprosencephaly
  • Holoprosencephaly sequence
  • Holoprosencephaly
  • Familial alobar holoprosencephaly
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteHead structure   69536005
parents
children
  • Agnathia, holoprosencephaly, situs inversus syndrome   722283003
  • Alobar holoprosencephaly   253137003
  • Cebocephaly   204052006
  • Ethmocephalus   55709000
  • Hartsfield syndrome   766032007
  • Holoprosencephaly and postaxial polydactyly syndrome   716091000
  • Holoprosencephaly craniosynostosis syndrome   715434005
  • Holoprosencephaly with caudal dysgenesis syndrome   771146007
  • Holoprosencephaly with nasal pyriformis aperture   890346002
  • Kundrat's syndrome   30278004
  • Lobar holoprosencephaly   253136007
  • Microform holoprosencephaly   1197215004
  • Middle interhemispheric variant of holoprosencephaly   866053004
  • Morse Rawnsley Sargent syndrome   716169009
  • Pancreatic agenesis, holoprosencephaly syndrome   1222660008
  • Semi-lobar holoprosencephaly   253138008
  • Steinfeld syndrome   716233007
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Congenital malformation   276654001
          Congenital malformation syndrome   400038003
            Malformation sequence   105989001
              Holoprosencephaly sequence   30915001

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of head   118934005
        Congenital anomaly of head   87290003
          Holoprosencephaly sequence   30915001

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.