Overview
Agenesis of corpus callosum is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Absence of corpus callosum
Very frequent (80-99%)HP:0001274
Deglutition disorder
Occasional (5-29%)HP:0002015
Dyslexia
Occasional (5-29%)HP:0010522
Dysorthography
Occasional (5-29%)HP:6000915
Incoordination
Occasional (5-29%)HP:0002311
Language impairment
Occasional (5-29%)HP:0002463
Mental retardation, severe
Occasional (5-29%)HP:0010864
Mental slowness
Occasional (5-29%)HP:0031843
Moderate mental retardation
Occasional (5-29%)HP:0002342
Peripheral hypotonia
Occasional (5-29%)HP:0001252
Poor attention span
Occasional (5-29%)HP:0000736
Specific learning disability
Occasional (5-29%)HP:0001328
Speech difficulties
Occasional (5-29%)HP:0000750
Bulging forehead
HP:0011220
Camptodactyly
HP:0012385
Contractures of the hands
HP:0009473
Decreased size of cranium
HP:0000252
Dull intelligence
HP:0001249
Frontal protuberance
HP:0002007
Growth failure
HP:0001510
Large head
HP:0000256
Preauricular skin tags
HP:0000384
Related Conditions
Agenesis of corpus callosum with lipoma(child)
Acrocallosal syndrome(child)
X-linked lissencephaly with abnormal genitalia syndrome(child)
Vici syndrome(child)
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome(child)
Infantile osteopetrosis with neuroaxonal dysplasia syndrome(child)
Agenesis of corpus callosum and abnormal genitalia syndrome(child)
Microcephaly, polymicrogyria, corpus callosum agenesis syndrome(child)
X-linked intellectual disability Kroes type(child)
7q36.3 microduplication syndrome(child)
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome(child)
Agenesis of corpus callosum with polyneuropathy(child)
Aplasia of corpus callosum(parent)
Quick Facts
- SNOMED CT
- 5102002
- UMLS CUI
- C0175754
- Fully Specified Name
- Agenesis of corpus callosum (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.