Myocardiopathy (congestive) (constrictive) (familial) (hypertrophic nonobstructive) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic)

"Myocardiopathy (congestive) (constrictive) (familial) (hypertrophic nonobstructive) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic)" 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 "myocardiopathy (congestive) (constrictive) (familial) (hypertrophic nonobstructive) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic)"

  • Myocardiopathy (congestive) (constrictive) (familial) (hypertrophic nonobstructive) (idiopathic) (infiltrative) (obstructive) (primary) (restrictive) (sporadic) - See Also: Cardiomyopathy; - I42.9 Cardiomyopathy, unspecified
    • alcoholic - I42.6 Alcoholic cardiomyopathy
    • cobalt-beer - I42.6 Alcoholic cardiomyopathy
    • glycogen storage - E74.02 Pompe disease
    • hypertrophic obstructive - I42.1 Obstructive hypertrophic cardiomyopathy
    • in (due to)
      • beriberi - E51.12 Wet beriberi
      • cardiac glycogenosis - E74.02 Pompe disease
      • 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
    • obscure (African) - I42.8 Other cardiomyopathies
    • secondary - I42.9 Cardiomyopathy, unspecified
    • thyrotoxic - E05.90 Thyrotoxicosis, unspecified without thyrotoxic crisis or storm
      • with storm - E05.91 Thyrotoxicosis, unspecified with thyrotoxic crisis or storm
    • toxic NEC - I42.7 Cardiomyopathy due to drug and external agent

Applicable Clinical Terms Definitions

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

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.