X-linked complicated corpus callosum dysgenesis 1010630006

SNOMED CT code

SNOMED code

1010630006

name

X-linked complicated corpus callosum dysgenesis

status

active

date introduced

2021-01-31

fully specified name(s)

X-linked complicated corpus callosum dysgenesis (disorder)

synonyms

X-linked complicated corpus callosum dysgenesis

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Associated morphology

Dilatation 25322007

Finding site

Brain cerebrospinal fluid pathway 280371009

attributes - group2

Finding site

Corpus callosum structure 88442005

Associated morphology

Hypoplasia 55199003

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

attributes - group3

Interprets

Intellectual ability 247573007

Has interpretation

Impaired 260379002

attributes - group4

Interprets

Adaptation behavior 406208005

Has interpretation

Impaired 260379002

parents

L1 syndrome 716996008

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Mental state, behavior and/or psychosocial function finding 384821006
Behavior finding 844005
Intellectual disability 110359009
L1 syndrome 716996008
X-linked complicated corpus callosum dysgenesis 1010630006

ancestors

sorted most to least specific

L1 syndrome 716996008
Intellectual disability 110359009
X-linked recessive hereditary disease 1162976004
Hypoplasia of corpus callosum 204043002
Developmental hereditary disorder 363070008
Hereditary disorder of nervous system 363235000
Multiple malformation syndrome with limb defect as major feature 41443008
Congenital hydrocephalus 47032000
Intellectual ability - finding 365814006
X-linked hereditary disease 128430005
Congenital malformation of corpus callosum 204042007
Multiple system malformation syndrome 82354003
Hydrocephalus 230745008
Impaired cognition 386806002
Neurodevelopmental disorder 700364009
Behavior finding 844005
Congenital hypoplasia of cerebrum 93249003
Hereditary disorder by system 363137000
Intelligence finding 106137004
Sex-linked hereditary disorder 82852009
Leukoencephalopathy 22811006
Congenital malformation syndrome 400038003
Cognitive function finding 373930000
Mental state, behavior and/or psychosocial function finding 384821006
Congenital anomaly of cerebrum 702628006
Congenital hypoplasia of part of brain 78693004
Functional finding 118228005
Hereditary disease 32895009
Finding of head region 298364001
Congenital hypoplasia of brain 127551000119100
Genetic disease 782964007
Congenital anomaly of brain 57148006
Disorder of brain 81308009
Congenital anomaly of central nervous system 128124001
Congenital anomaly of head 87290003
Disorder of head 118934005
Disorder of the central nervous system 23853001
Finding of brain 299718000
Congenital anomaly of nervous system 88425004
Head finding 406122000
Disorder of nervous system 118940003
Congenital malformation 276654001
Central nervous system finding 246556002
Finding of head and neck region 118254002
Disorder of body system 362965005
Developmental disorder 5294002
Congenital disease 66091009
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Mental state, behavior and/or psychosocial function finding 384821006

Behavior finding 844005

Intellectual disability 110359009

L1 syndrome 716996008

X-linked complicated corpus callosum dysgenesis 1010630006

SNOMED CT code