Cardiomyopathy (familial) (idiopathic)

"Cardiomyopathy (familial) (idiopathic)" References in the ICD-10-CM Index to Diseases and Injuries

References in the ICD-10-CM Index to Diseases and Injuries applicable to the clinical term "cardiomyopathy (familial) (idiopathic)"

  • Cardiomyopathy (familial) (idiopathic) - I42.9 Cardiomyopathy, unspecified
    • alcoholic - I42.6 Alcoholic cardiomyopathy
    • amyloid - E85.4 Organ-limited amyloidosis
    • arteriosclerotic - See: Disease, heart, ischemic, atherosclerotic;
    • beriberi - E51.12 Wet beriberi
    • cobalt-beer - I42.6 Alcoholic cardiomyopathy
    • congenital - I42.4 Endocardial fibroelastosis
    • congestive - I42.0 Dilated cardiomyopathy
    • constrictive NOS - I42.5 Other restrictive cardiomyopathy
    • dilated - I42.0 Dilated cardiomyopathy
    • due to
      • alcohol - I42.6 Alcoholic cardiomyopathy
      • beriberi - E51.12 Wet beriberi
      • cardiac glycogenosis - E74.02 Pompe disease
      • drugs - I42.7 Cardiomyopathy due to drug and external agent
      • external agents NEC - I42.7 Cardiomyopathy due to drug and external agent
      • Friedreich's ataxia - G11.1 Early-onset cerebellar ataxia
      • myotonia atrophica - G71.11 Myotonic muscular dystrophy
      • progressive muscular dystrophy - G71.09 Other specified muscular dystrophies
    • glycogen storage - E74.02 Pompe disease
    • hypertensive - See: Hypertension, heart;
    • hypertrophic (nonobstructive) - I42.2 Other hypertrophic cardiomyopathy
      • obstructive - I42.1 Obstructive hypertrophic cardiomyopathy
        • congenital - Q24.8 Other specified congenital malformations of heart
    • in
      • Chagas' disease (chronic) - B57.2 Chagas' disease (chronic) with heart involvement
        • acute - B57.0 Acute Chagas' disease with heart involvement
      • sarcoidosis - D86.85 Sarcoid myocarditis
    • ischemic - I25.5 Ischemic cardiomyopathy
    • metabolic - E88.9 Metabolic disorder, unspecified
      • thyrotoxic - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
        • with thyroid storm - E05.91 Thyrotoxicosis, unspecified with thyrotoxic crisis or storm
    • newborn - I42.8 Other cardiomyopathies
      • congenital - I42.4 Endocardial fibroelastosis
    • non-ischemic - See Also: by cause; - I42.8 Other cardiomyopathies
    • nutritional - E63.9 Nutritional deficiency, unspecified
      • beriberi - E51.12 Wet beriberi
    • obscure of Africa - I42.8 Other cardiomyopathies
    • peripartum - O90.3 Peripartum cardiomyopathy
    • postpartum - O90.3 Peripartum cardiomyopathy
    • restrictive NEC - I42.5 Other restrictive cardiomyopathy
    • rheumatic - I09.0 Rheumatic myocarditis
    • secondary - I42.9 Cardiomyopathy, unspecified
    • specified NEC - I42.8 Other cardiomyopathies
    • stress induced - I51.81 Takotsubo syndrome
    • takotsubo - I51.81 Takotsubo syndrome
    • thyrotoxic - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
      • with thyroid storm - E05.91 Thyrotoxicosis, unspecified with thyrotoxic crisis or storm
    • toxic NEC - I42.7 Cardiomyopathy due to drug and external agent
    • tuberculous - A18.84 Tuberculosis of heart
    • viral - B33.24 Viral cardiomyopathy

Applicable Clinical Terms Definitions

Alcoholics: Persons who have a history of physical or psychological dependence on ETHANOL.

Amyloid: A fibrous protein complex that consists of proteins folded into a specific cross beta-pleated sheet structure. This fibrillar structure has been found as an alternative folding pattern for a variety of functional proteins. Deposits of amyloid in the form of AMYLOID PLAQUES are associated with a variety of degenerative diseases. The amyloid structure has also been found in a number of functional proteins that are unrelated to disease.

Beriberi: A disease caused by a deficiency of thiamine (vitamin B1) and characterized by polyneuritis, cardiac pathology, and edema. The epidemic form is found primarily in areas in which white (polished) rice is the staple food, as in Japan, China, the Philippines, India, and other countries of southeast Asia. (Dorland, 27th ed)

Friedreich Ataxia: An autosomal recessive disease, usually of childhood onset, characterized pathologically by degeneration of the spinocerebellar tracts, posterior columns, and to a lesser extent the corticospinal tracts. Clinical manifestations include GAIT ATAXIA, pes cavus, speech impairment, lateral curvature of spine, rhythmic head tremor, kyphoscoliosis, congestive heart failure (secondary to a cardiomyopathy), and lower extremity weakness. Most forms of this condition are associated with a mutation in a gene on chromosome 9, at band q13, which codes for the mitochondrial protein frataxin. (From Adams et al., Principles of Neurology, 6th ed, p1081; N Engl J Med 1996 Oct 17;335(16):1169-75) The severity of Friedreich ataxia associated with expansion of GAA repeats in the first intron of the frataxin gene correlates with the number of trinucleotide repeats. (From Durr et al, N Engl J Med 1996 Oct 17;335(16):1169-75)

Myotonic Dystrophy: Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2.

Infant, Newborn: An infant during the first 28 days after birth.

Postpartum Period: In females, the period that is shortly after giving birth (PARTURITION).

Sarcoidosis: An idiopathic systemic inflammatory granulomatous disorder comprised of epithelioid and multinucleated giant cells with little necrosis. It usually invades the lungs with fibrosis and may also involve lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands.