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Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
disorderSNOMED 773398005CUI C4750835
Overview
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay 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.
Abnormal muscle fiber protein expression
Frequent (30-79%)HP:0030089
Central hypotonia
Frequent (30-79%)HP:0001252
Cognitive delay
Frequent (30-79%)HP:0001263
Congenital cataracts, bilateral
Frequent (30-79%)HP:0000519
Decreased circulating ferritin concentration
Frequent (30-79%)HP:0012343
Eyelid ptosis
Frequent (30-79%)HP:0000508
Hypoplasia of corpus callosum
Frequent (30-79%)HP:0002079
Lacticacidemia
Frequent (30-79%)HP:0003128
Progressive sensorineural hearing impairment
Frequent (30-79%)HP:0000408
Reduced tendon reflexes
Frequent (30-79%)HP:0001315
Rotary nystagmus
Frequent (30-79%)HP:0001583
Truncal hypotonia
Frequent (30-79%)HP:0008936
Related Conditions
Hereditary disorder of the visual system(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital cataract(parent)
Mitochondrial myopathy(parent)
Developmental delay(parent)
Congenital sensorineural hearing loss(parent)
Hereditary disorder of musculoskeletal system(parent)
Developmental hereditary disorder(parent)
Hereditary hearing loss(parent)
Quick Facts
- SNOMED CT
- 773398005
- UMLS CUI
- C4750835
- Fully Specified Name
- Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 12
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.