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Congenital cataract, nephropathy, encephalopathy syndrome

disorder
SNOMED 722381004CUI C0795914

Overview

Congenital cataract, nephropathy, encephalopathy 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.

Cataract, congenital
Always present (100%)HP:0000519
Cerebellar dysplasia
Always present (100%)HP:0007033
Decreased size of cranium
Always present (100%)HP:0000252
Global developmental delay, severe
Always present (100%)HP:0011344
Renal tubular epithelial necrosis
Always present (100%)HP:0008682
Decreased body height
Very frequent (80-99%)HP:0004322
Epilepsy
Very frequent (80-99%)HP:0001250
Lens opacities
Very frequent (80-99%)HP:0000518
Nonprogressive mental retardation
Very frequent (80-99%)HP:0001249
Renal tubular defect
Very frequent (80-99%)HP:0000124
Involuntary, rapid, rhythmic eye movements
Frequent (30-79%)HP:0000639

Quick Facts

SNOMED CT
722381004
UMLS CUI
C0795914
Fully Specified Name
Congenital cataract, nephropathy, encephalopathy syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
11
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.