G71.2 Sarcotubular myopathy (disorder)

Search
Generic filters

Sarcotubular myopathy (disorder)

Sarcotubular myopathy (disorder)
Synonym for Congenital myopathies

    G00-G99 Diseases of the nervous system (G00-G99)|G70-G73 Diseases of myoneural junction and muscle (G70-G73)|G71 Primary disorders of muscles

Results for Sarcotubular myopathy (disorder) and additional synonyms


G71.2
Congenital myopathies

Synonyms:

Actin accumulation myopathy|Actin accumulation myopathy (disorder)|Autosomal recessive centronuclear myopathy|Autosomal recessive centronuclear myopathy (disorder)|Benign congenital myopathy|Benign congenital myopathy (disorder)|Cap disease|Cap myopathy|Cap myopathy (disorder)|Carey Fineman Ziter syndrome|Central core disease|Central core disease (disorder)|Central core myopathy|Centronuclear myopathy|Congenital anomaly of skeletal muscle|Congenital anomaly of skeletal muscle (disorder)|Congenital hereditary muscular dystrophy|Congenital hereditary muscular dystrophy (disorder)|Congenital myopathy with abnormal subcellular organelles|Congenital myopathy with abnormal subcellular organelles (disorder)|Congenital myopathy with caps|Congenital myopathy with excess thin filaments|Congenital myopathy with fiber type disproportion|Congenital myopathy with fiber type disproportion (disorder)|Congenital myopathy with fibre type disproportion|Congenital myopathy with uniform fiber type|Congenital myopathy with uniform fiber type (disorder)|Congenital myopathy with uniform fibre type|Congenital nonprogressive myopathy with Moebius and Robin sequences|Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder)|Fiber-type disproportion|IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia|Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia|Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)|Lower motor neuron degeneration with Paget-like bone disease|Minicore disease|Minimal change myopathy|Minimal change myopathy (disorder)|Mixed congenital myopathy|Mixed congenital myopathy (disorder)|Multi-core congenital myopathy|Multi-core congenital myopathy (disorder)|Multi-core disease|Multi-minicore disease|Multicore disease|Multiminicore disease|Muscular dystrophy limb-girdle with Paget disease of bone|Myopathy with abnormality of histochemical fiber type|Myopathy with abnormality of histochemical fiber type (disorder)|Myopathy with abnormality of histochemical fibre type|Myopathy with cytoplasmic inclusions|Myopathy with cytoplasmic inclusions (disorder)|Myopathy with tubular aggregates|Myopathy with tubular aggregates (disorder)|Myopathy with type I hypotrophy|Myopathy with type I hypotrophy (disorder)|Myotubular (centronuclear) myopathy|Myotubular myopathy|Myotubular myopathy (disorder)|Myotubular myopathy with type I atrophy|Myotubular myopathy with type I atrophy (disorder)|Nemaline body disease|Nemaline myopathy|Nemaline myopathy (disorder)|Nemaline myopathy 3|Nemaline myopathy, early onset type|Nemaline myopathy, early onset type (disorder)|Nemaline myopathy, late onset type|Nemaline myopathy, late onset type (disorder)|Pagetoid amyotrophic lateral sclerosis|Pagetoid neuroskeletal syndrome|Reducing-body myopathy|Reducing-body myopathy (disorder)|Rod myopathy|Rod-body myopathy|Sarcotubular myopathy|Sarcotubular myopathy (disorder)|Severe x-linked myotubular myopathy|Severe x-linked myotubular myopathy (disorder)|X-linked centronuclear myopathy|Zebra body myopathy|Zebra body myopathy (disorder)

Subcategories:

    All content of the ICD-10 CM Search is based on the classifications and codes of the Centers for Medicare and Medicaid Services (CMS) and the National Center for Health Statistics (NCHS). The accumulation of synonyms is carried out by Averbis GmbH with Healthcare Natural Language Processing. All information is provided without guarantee. Errors and omissions excepted. We expressly reserve the right to make changes, additions or deletions to the information or links provided at any time without prior notice. Our offer is non-binding. For correctness, completeness and topicality or designations no liability is assumed.

    ICD-Search ICD 10 CM (Clinical Modification) 2017 through Healthcare Natural Language Processing & Deep Learning

    ICD-Code / International Statistical Classification of Diseases and Related Health Problems (ICD) for: Sarcotubular myopathy (disorder)

    ICD Code for Disease, Diagnosis G71.2

    ICD Code an Classification Congenital myopathies

    Chapter, Outline, Main Categories, Parent Concepts or Top Concepts: G00-G99 Diseases of the nervous system (G00-G99)|G70-G73 Diseases of myoneural junction and muscle (G70-G73)|G71 Primary disorders of muscles

    Subcategories, subconcepts or child concepts:

    Synonyms:

    Synonyms: G71.2: Sarcotubular myopathy (disorder)

    Other Synonyms of the Category: Actin accumulation myopathy|Actin accumulation myopathy (disorder)|Autosomal recessive centronuclear myopathy|Autosomal recessive centronuclear myopathy (disorder)|Benign congenital myopathy|Benign congenital myopathy (disorder)|Cap disease|Cap myopathy|Cap myopathy (disorder)|Carey Fineman Ziter syndrome|Central core disease|Central core disease (disorder)|Central core myopathy|Centronuclear myopathy|Congenital anomaly of skeletal muscle|Congenital anomaly of skeletal muscle (disorder)|Congenital hereditary muscular dystrophy|Congenital hereditary muscular dystrophy (disorder)|Congenital myopathy with abnormal subcellular organelles|Congenital myopathy with abnormal subcellular organelles (disorder)|Congenital myopathy with caps|Congenital myopathy with excess thin filaments|Congenital myopathy with fiber type disproportion|Congenital myopathy with fiber type disproportion (disorder)|Congenital myopathy with fibre type disproportion|Congenital myopathy with uniform fiber type|Congenital myopathy with uniform fiber type (disorder)|Congenital myopathy with uniform fibre type|Congenital nonprogressive myopathy with Moebius and Robin sequences|Congenital nonprogressive myopathy with Moebius and Robin sequences (disorder)|Fiber-type disproportion|IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia|Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia|Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)|Lower motor neuron degeneration with Paget-like bone disease|Minicore disease|Minimal change myopathy|Minimal change myopathy (disorder)|Mixed congenital myopathy|Mixed congenital myopathy (disorder)|Multi-core congenital myopathy|Multi-core congenital myopathy (disorder)|Multi-core disease|Multi-minicore disease|Multicore disease|Multiminicore disease|Muscular dystrophy limb-girdle with Paget disease of bone|Myopathy with abnormality of histochemical fiber type|Myopathy with abnormality of histochemical fiber type (disorder)|Myopathy with abnormality of histochemical fibre type|Myopathy with cytoplasmic inclusions|Myopathy with cytoplasmic inclusions (disorder)|Myopathy with tubular aggregates|Myopathy with tubular aggregates (disorder)|Myopathy with type I hypotrophy|Myopathy with type I hypotrophy (disorder)|Myotubular (centronuclear) myopathy|Myotubular myopathy|Myotubular myopathy (disorder)|Myotubular myopathy with type I atrophy|Myotubular myopathy with type I atrophy (disorder)|Nemaline body disease|Nemaline myopathy|Nemaline myopathy (disorder)|Nemaline myopathy 3|Nemaline myopathy, early onset type|Nemaline myopathy, early onset type (disorder)|Nemaline myopathy, late onset type|Nemaline myopathy, late onset type (disorder)|Pagetoid amyotrophic lateral sclerosis|Pagetoid neuroskeletal syndrome|Reducing-body myopathy|Reducing-body myopathy (disorder)|Rod myopathy|Rod-body myopathy|Sarcotubular myopathy|Sarcotubular myopathy (disorder)|Severe x-linked myotubular myopathy|Severe x-linked myotubular myopathy (disorder)|X-linked centronuclear myopathy|Zebra body myopathy|Zebra body myopathy (disorder)

    ICD 10 CM 2017, (Clinical Modification) for coding of death certificates and mortality data. The international Statistical Classification of Diseases and Related Health Problems (ICD) 10th Revision and Clinical Modification. International Classification of Diseases, Tenth Revision, Clinical Modification.G71.2 Congenital myopathies and Sarcotubular myopathy (disorder)

    Sarcotubular myopathy (disorder)
    Written by: on
    Averbis GmbH

    Jetzt weitere Informationen und Demo anfordern!

    kostenlos & unverbindlich

    Schreiben Sie uns von Ihrem Vorhaben (Pflichtfeld)

    Anwendungsgebiet
    HealthcarePatentePharmaAndere

    Vorname (Pflichtfeld)

    Name (Pflichtfeld)


    Jobtitle / Rolle (Pflichtfeld)

    Firma (Pflichtfeld)

    E-Mail-Adresse (Pflichtfeld)

    Telefon

    GET MORE INFORMATION

    Your message (required)

    Use case
    HealthcarePatentsPharmaOthers

    First Name (required)

    Last Name (required)


    Job Title / Role (required)

    Company (required)

    Email (required)

    Phone