Congenital anomaly of brain
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Congenital anomaly of cerebrum (disorder)
Congenital anomaly of cerebrum
congenitale afwijking van cerebrum
Id702628006
StatusDefined
Associated morphologyMorphologically abnormal structure
Finding siteCerebrum
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetQ04.9
RuleTRUE
AdviceALWAYS Q04.9
CorrelationSNOMED CT source code to target map code correlation not specified
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Absence of septum pellucidum
Agenesis of cerebrum
Alobar holoprosencephaly
Anomalies of hypothalamus1
Arhinencephaly
Atelencephaly
Bilateral frontal polymicrogyria
Bilateral frontoparietal polymicrogyria
Bilateral generalized polymicrogyria
Bilateral parasagittal parieto-occipital polymicrogyria
CEDNIK syndrome
Cerebral cortical dysgenesis
Colpocephaly
Congenital abnormal shape of cerebrum
Congenital achiasma
Congenital cerebral hernia
Congenital hypoplasia of cerebrum5
Congenital malformation of corpus callosum5
Congenital porencephalic cyst
Cortical dysplasia4
Craniosynostosis and intracranial calcification syndrome
Cystic leukoencephalopathy without megalencephaly
Defect of telencephalic division
Diencephalic mesencephalic junction dysplasia
Ectopic gray matter in centrum ovale
Encephalopathy, intracerebral calcification, retinal degeneration syndrome
Endocrine-cerebro-osteodysplasia syndrome
Epileptic encephalopathy with global cerebral demyelination
Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome
Hemispheric cerebral agenesis
Hydranencephaly3
Isolated arhinencephaly
Keratosis follicularis, dwarfism, cerebral atrophy syndrome
Kundrat's syndrome
Lethal occipital encephalocele, skeletal dysplasia syndrome
Lissencephaly due to LIS1 mutation
Lobar holoprosencephaly
Macroencephaly8
Macrogyria4
Microcephalic cortical malformations, short stature due to RTTN deficiency
Microdysgenesis
Middle interhemispheric variant of holoprosencephaly
Partial absence of septum pellucidum
Polymicrogyria due to TUBB2B mutation
Schizencephaly
Semi-lobar holoprosencephaly
Status marmoratus
Subcortical nodular heterotopia
Tubulinopathy-associated dysgyria
Visceral neuropathy and brain anomaly with facial dysmorphism and developmental delay syndrome
Worster Drought syndrome
Zechi Ceide syndrome