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Microcephaly, thin corpus callosum, intellectual disability syndrome

disorder
SNOMED 770721009CUI C4749429

Overview

Microcephaly, thin corpus callosum, intellectual disability syndrome 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.

Cognitive delay
Frequent (30-79%)HP:0001263
Corticospinal signs
Frequent (30-79%)HP:0007256
Delayed myelination
Frequent (30-79%)HP:0012448
Difficulty speaking
Frequent (30-79%)HP:0002465
Extensor plantar responses
Frequent (30-79%)HP:0003487
Hypoplasia of corpus callosum
Frequent (30-79%)HP:0002079
Increased reflexes
Frequent (30-79%)HP:0001347
Involuntary muscle stiffness, contraction, or spasm
Frequent (30-79%)HP:0001257
Mental-retardation
Frequent (30-79%)HP:0001249
Nonverbal
Frequent (30-79%)HP:0001344
Postnatal microcephaly
Frequent (30-79%)HP:0005484
Abnormality of the feet
Occasional (5-29%)HP:0001760
Bicuspid aortic valve
Occasional (5-29%)HP:0001647
Cerebral atrophy
Occasional (5-29%)HP:0002059
Horizontal nystagmus
Occasional (5-29%)HP:0000666
Nonsyndromal hydrocephalus
Occasional (5-29%)HP:0000238
Outward facing eye ball
Occasional (5-29%)HP:0000577
Retinal pigmentary anomaly
Occasional (5-29%)HP:0007703

Quick Facts

SNOMED CT
770721009
UMLS CUI
C4749429
Fully Specified Name
Microcephaly, thin corpus callosum, intellectual disability syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
18
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.