Acrocephalopolysyndactyly type II 403767009

SNOMED CT code

SNOMED code

403767009

name

Acrocephalopolysyndactyly type II

status

active

date introduced

2003-07-31

fully specified name(s)

Acrocephalopolysyndactyly type II (disorder)

synonyms

Acrocephalopolysyndactyly type II
Carpenter syndrome
Acrocephalopolysyndactyly type 2

attributes - group1

Pathological process

Pathological developmental process 308490002

Finding site

Digit structure 82680008

Associated morphology

Congenital abnormal fusion 37764001

Occurrence

Congenital 255399007

attributes - group2

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Congenital premature fusion 67798003

Finding site

Joint structure of suture of skull 51863000

attributes - group3

Associated morphology

Supernumerary structure 91431006

Finding site

Digit structure 82680008

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

parents

Acrocephalopolysyndactyly 205260006
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Autosomal recessive hereditary disorder 85995004

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Acrocephalosyndactyly 268262006
Acrocephalopolysyndactyly 205260006
Acrocephalopolysyndactyly type II 403767009

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Acrocephalopolysyndactyly type II 403767009

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Disorder of musculoskeletal system 928000
Hereditary disorder of musculoskeletal system 363212003
Acrocephalopolysyndactyly type II 403767009

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal recessive hereditary disorder 85995004
Acrocephalopolysyndactyly type II 403767009

ancestors

sorted most to least specific

Acrocephalopolysyndactyly 205260006
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Autosomal recessive hereditary disorder 85995004
Acrocephalosyndactyly 268262006
Hereditary disorder by system 363137000
Autosomal hereditary disorder 1899006
Polysyndactyly 84598000
Syndactyly 373413006
Hereditary disease 32895009
Polydactyly 367506006
Multiple malformation syndrome with limb defect as major feature 41443008
Craniosynostosis syndrome 57219006
Congenital anomaly of digit 403855001
Genetic disease 782964007
Multiple system malformation syndrome 82354003
Imperfect fusion of skull 23939000
Polymelia 89243009
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

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Genetic disease 782964007

Acrocephalosyndactyly 268262006

Acrocephalopolysyndactyly 205260006

Acrocephalopolysyndactyly type II 403767009

SNOMED CT code