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Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome

disorder
SNOMED 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

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.