Overview
Raynaud Claes 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.
Central hypotonia
Always present (100%)HP:0001252
Dystonic movements
Always present (100%)HP:0001332
Epileptic encephalopathy
Always present (100%)HP:0200134
Psychomotor development deficiency
Very frequent (80-99%)HP:0001263
Abnormality of the cerebral white matter
Frequent (30-79%)HP:0002500
Cerebral cortex atrophy
Frequent (30-79%)HP:0002120
Epilepsy
Frequent (30-79%)HP:0001250
Mental retardation, severe
Frequent (30-79%)HP:0010864
Moderate mental retardation
Frequent (30-79%)HP:0002342
Autism spectrum disorder
Occasional (5-29%)HP:0000729
Autoagression
Occasional (5-29%)HP:0100716
Behavioral symptoms
Occasional (5-29%)HP:0000708
Bipolar depression
Occasional (5-29%)HP:0007302
Cobb angle greater than ten degrees
Occasional (5-29%)HP:0002650
Complex partial seizures
Occasional (5-29%)HP:0002384
CVI
Occasional (5-29%)HP:0100704
Decreased size of cranium
Occasional (5-29%)HP:0000252
Delayed myelination
Occasional (5-29%)HP:0012448
Depression
Occasional (5-29%)HP:0000716
Dilated cerebral ventricle
Occasional (5-29%)HP:0002119
EEG with focal spikes
Occasional (5-29%)HP:0011193
Excessive, persistent worry and fear
Occasional (5-29%)HP:0000739
Feeding difficulties
Occasional (5-29%)HP:0011968
Focal tonic seizure
Occasional (5-29%)HP:0011167
Gastro-esophageal reflux
Occasional (5-29%)HP:0002020
Generalized non-motor (absence) seizure
Occasional (5-29%)HP:0002121
Generalized tonic-clonic seizure (without specification of onset)
Occasional (5-29%)HP:0002069
hyperkinetic disorder
Occasional (5-29%)HP:0000752
Hypoplasia of corpus callosum
Occasional (5-29%)HP:0002079
Hypotonia, early
Occasional (5-29%)HP:0008947
Quick Facts
- SNOMED CT
- 1172691004
- UMLS CUI
- C0796221
- Fully Specified Name
- Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.