Progressive cerebello-cerebral atrophy

disorder

SNOMED 1208481000CUI C3151140

Overview

Progressive cerebello-cerebral atrophy 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.

Appendicular spasticity

Always present (100%)HP:0034353

Cognitive delay

Always present (100%)HP:0001263

Paroxysmal tonic upgaze

Always present (100%)HP:0033980

Seizures

Always present (100%)HP:0001250

Vermian atrophy

Always present (100%)HP:0006855

Abnormality of the periventricular white matter

HP:0002518

Choreatic disease

HP:0002072

Clonus

HP:0002169

Degeneration of cerebellum

HP:0001272

Degeneration of cerebrum

HP:0002059

Delayed myelination

HP:0012448

Hypoplasia of corpus callosum

HP:0002079

Intellectual disability, profound

HP:0002187

Irritability

HP:0000737

Limb joint contracture

HP:0003121

Microcephaly, progressive

HP:0000253

Spastic quadriplegia

HP:0002510

Trouble sleeping

HP:0002360

Related Conditions

Global developmental delay(parent)

Cerebral atrophy(parent)

Developmental hereditary disorder(parent)

Chronic brain syndrome(parent)

Recessive hereditary disorder (autosomal)(parent)

Genetic intellectual disability(parent)

Hereditary cerebellar atrophy(parent)

Quick Facts

SNOMED CT: 1208481000
UMLS CUI: C3151140
Fully Specified Name: Progressive cerebello-cerebral atrophy (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.