Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT code

SNOMED code

726724005

name

Splenogonadal fusion, limb defect, micrognathia syndrome

status

active

date introduced

2017-07-31

fully specified name(s)

Splenogonadal fusion, limb defect, micrognathia syndrome (disorder)

synonyms

Splenogonadal fusion, limb defect, micrognathia syndrome
SGFLD (splenogonadal fusion limb defect syndrome) syndrome
Splenogonadal fusion limb defect syndrome

attributes - group5

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Finding site

Bone structure 272673000

Associated morphology

Dysplasia 25723000

attributes - group3

Associated morphology

Congenital abnormal fusion 37764001

Finding site

Gonadal structure 43174007

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Finding site

Bone structure of mandible 91609006

Associated morphology

Hypoplasia 55199003

attributes - group4

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Abnormally short growth 11182007

Finding site

Entire limb 243996003

attributes - group2

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Congenital abnormal fusion 37764001

Finding site

Splenic structure 78961009

parents

Dysostosis 109420003
Autosomal dominant hereditary disorder 11164009
Multiple malformation syndrome with facial-limb defects as major feature 23359005
Congenital micrognathism 32958008
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Reproductive system hereditary disorder 363290007
Splenogonadal fusion 62042001
Longitudinal deficiency of limb 67341007

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Disorder of bone development 371521007
Congenital anomaly of skeletal bone 8447006
Dysostosis 109420003
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of limb structure 302293008
Disorder of limb 128605003
Congenital anomaly of limb 60475009
Multiple malformation syndrome with facial-limb defects as major feature 23359005
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of head 118934005
Disorder of jaw 37156001
Congenital anomaly of jaw 95473006
Congenital anomaly of mandible 128224008
Congenital micrognathism 32958008
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Musculoskeletal finding 106028002
Disorder of musculoskeletal system 928000
Hereditary disorder of musculoskeletal system 363212003
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of body system 362965005
Hereditary disorder by system 363137000
Reproductive system hereditary disorder 363290007
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Viscus structure finding 406123005
Abdominal organ finding 249561001
Disorder of spleen 51244008
Lesion of spleen 141701000119101
Splenogonadal fusion 62042001
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT Concept 138875005
Clinical finding 404684003
Finding of limb structure 302293008
Deformity of limb 445144002
Longitudinal deficiency of limb 67341007
Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

ancestors

sorted most to least specific

Dysostosis 109420003
Autosomal dominant hereditary disorder 11164009
Multiple malformation syndrome with facial-limb defects as major feature 23359005
Congenital micrognathism 32958008
Developmental hereditary disorder 363070008
Hereditary disorder of musculoskeletal system 363212003
Reproductive system hereditary disorder 363290007
Splenogonadal fusion 62042001
Longitudinal deficiency of limb 67341007
Skeletal dysplasia 105986008
Autosomal hereditary disorder 1899006
Multiple malformation syndrome with limb defect as major feature 41443008
Congenital anomaly of mandible 128224008
Hereditary disorder by system 363137000
Lesion of spleen 141701000119101
Congenital deformity 276655000
Congenital anomaly of limb 60475009
Multiple malformation syndrome with facial defects as major feature 65094009
Craniofacial microsomia 254026007
Hypoplasia of mandibular bone 444897001
Gonadal dysgenesis 205681004
Congenital anomaly of spleen 57497006
Lesion of genitalia 724386005
Deformity of limb 445144002
Hereditary disease 32895009
Multiple system malformation syndrome 82354003
Disorder of spleen 51244008
Disorder of limb 128605003
Mandibular jaw size anomaly 235080003
Congenital anomaly of face bones 32003007
Congenital anomaly of jaw 95473006
Congenital malformation of genital organs 204821009
Congenital anomaly of abdomen 363024001
Deformity 417893002
Congenital anomaly of the hematopoietic system 40888008
Genetic disease 782964007
Congenital malformation syndrome 400038003
Disorder of mandible 128233005
Disorder of reproductive system 362968007
Disorder of lymphoid system 111590001
Finding of limb structure 302293008
Congenital anomaly of face 398302004
Congenital abnormality of skull and face bones 268239009
Genitourinary congenital anomalies 287085006
Disorder of abdomen 118948005
Genital finding 300479008
Abdominal organ finding 249561001
Anomaly of jaw size 323351000119108
Disorder of facial bone 128225009
Disorder of the genitourinary system 42030000
Disorder of hematopoietic structure 414027002
Congenital anomaly of skeletal bone 8447006
Disorder of jaw 37156001
Congenital anomaly of lower trunk 363030001
Finding of abdomen 609624008
Viscus structure finding 406123005
Disorder of immune structure 414030009
Congenital anomaly of head 87290003
Congenital anomaly of musculoskeletal system 73573004
Disorder of face 118930001
Urogenital finding 118238000
Disorder of bone development 371521007
Facial bone finding 248398006
Disorder of abdominopelvic segment of trunk 822988000
Congenital abnormality of lower limb and pelvic girdle 253937004
Congenital anomaly of trunk 78626001
Congenital malformation 276654001
Disorder of head 118934005
Finding of abdominopelvic segment of trunk 822987005
Disorder of bone 76069003
Finding of face 301310005
Disorder of trunk 128121009
Developmental disorder 5294002
Finding of trunk structure 302292003
Disorder of skeletal system 88230002
Congenital disease 66091009
Bone finding 118953000
Finding of head region 298364001
Head finding 406122000
Disorder of musculoskeletal system 928000
Finding of head and neck region 118254002
Disorder of body system 362965005
Musculoskeletal finding 106028002
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Developmental disorder 5294002

Disorder of bone development 371521007

Congenital anomaly of skeletal bone 8447006

Dysostosis 109420003

Splenogonadal fusion, limb defect, micrognathia syndrome 726724005

SNOMED CT code