Pfeiffer syndrome type 2 1003916008

SNOMED CT code

SNOMED code

1003916008

name

Pfeiffer syndrome type 2

status

active

date introduced

2021-01-31

fully specified name(s)

Pfeiffer syndrome type 2 (disorder)

synonyms

Pfeiffer syndrome type 2

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Associated morphology

Congenital abnormal fusion 37764001

Finding site

Digit structure 82680008

attributes - group2

Associated morphology

Congenital premature fusion 67798003

Occurrence

Congenital 255399007

Finding site

Joint structure of suture of skull 51863000

Pathological process

Pathological developmental process 308490002

parents

Acrocephalosyndactyly type V 70410008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Acrocephalosyndactyly 268262006
Acrocephalosyndactyly type V 70410008
Pfeiffer syndrome type 2 1003916008

ancestors

sorted most to least specific

Acrocephalosyndactyly type V 70410008
Autosomal dominant hereditary disorder 11164009
Acrocephalosyndactyly 268262006
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Autosomal hereditary disorder 1899006
Syndactyly 373413006
Hereditary disorder by system 363137000
Multiple malformation syndrome with limb defect as major feature 41443008
Craniosynostosis syndrome 57219006
Hereditary disease 32895009
Congenital anomaly of digit 403855001
Multiple system malformation syndrome 82354003
Imperfect fusion of skull 23939000
Genetic disease 782964007
Disorder of digit 128597007
Congenital malformation syndrome 400038003
Cranial suture finding 248387005
Congenital anomaly of limb 60475009
Lesion of joint 298149009
Congenital anomaly of head 87290003
Congenital anomaly of joint 95463009
Disorder of limb 128605003
Arthropathy 399269003
Disorder of head 118934005
Congenital anomaly of musculoskeletal system 73573004
Finding of limb structure 302293008
Congenital malformation 276654001
Joint finding 118952005
Head finding 406122000
Disorder of joint region 785875003
Disorder of skeletal system 88230002
Developmental disorder 5294002
Disorder of musculoskeletal system 928000
Congenital disease 66091009
Finding of head and neck region 118254002
Musculoskeletal finding 106028002
Disorder of body system 362965005
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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

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

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Acrocephalosyndactyly 268262006

Acrocephalosyndactyly type V 70410008

Pfeiffer syndrome type 2 1003916008

SNOMED CT code