Myopathy and diabetes mellitus

disorder

SNOMED 783722008CUI C5191051

Overview

Myopathy and diabetes mellitus 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.

Skeletal myopathy

Very frequent (80-99%)HP:0003756

Symmetrical, proximal limb muscle atrophy

Very frequent (80-99%)HP:0007126

Type I diabetes mellitus

Very frequent (80-99%)HP:0100651

Difficulty running

Frequent (30-79%)HP:0009046

Difficulty walking up stairs

Frequent (30-79%)HP:0003551

Extensor plantar responses

Frequent (30-79%)HP:0003487

Hyporeflexia of upper limbs

Frequent (30-79%)HP:0012391

Inability to walk

Frequent (30-79%)HP:0002540

Lower limb hyperreflexia

Frequent (30-79%)HP:0002395

Muscle weakness, progressive, proximal

Frequent (30-79%)HP:0009073

Poor exercise tolerance

Frequent (30-79%)HP:0003546

Shoulder weakness

Frequent (30-79%)HP:0003547

Difficulty articulating speech

Occasional (5-29%)HP:0001260

Frequent falls

Occasional (5-29%)HP:0002359

Hip-girdle muscle weakness

Occasional (5-29%)HP:0003749

Laboured breathing

Occasional (5-29%)HP:0002098

Lower limb atrophy

Occasional (5-29%)HP:0008944

Moderate mental retardation

Occasional (5-29%)HP:0002342

Muscle pain

Occasional (5-29%)HP:0003326

Peripheral axonal neuropathy

Occasional (5-29%)HP:0003477

Progressive cerebellar ataxia

Occasional (5-29%)HP:0002073

Sternocleidomastoid amyotrophy

Occasional (5-29%)HP:0012036

Walking on tiptoes

Occasional (5-29%)HP:0030051

Weakness of face

Occasional (5-29%)HP:0030319

Weakness of orbicularis oculi muscle

Occasional (5-29%)HP:0012507

Achilles tendon contracture

Very rare (1-4%)HP:0001771

Altered consciousness or cognition

Very rare (1-4%)HP:0031258

Hypotonia, in neonatal onset

Very rare (1-4%)HP:0001319

Impaired vibratory sensation

Very rare (1-4%)HP:0002495

Progressive dementia

Very rare (1-4%)HP:0000726

Related Conditions

Mitochondrial myopathy(parent)

Diabetes mellitus associated with genetic syndrome(parent)

Genetic disease(parent)

Quick Facts

SNOMED CT: 783722008
UMLS CUI: C5191051
Fully Specified Name: Myopathy and diabetes mellitus (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.