ICD-10-CM Dystrophy, dystrophia References
"Dystrophy, dystrophia" Annotation Back-References in the ICD-10-CM Index to Diseases and Injuries
Browse the ICD-10-CM codes with references applicable to the clinical term "dystrophy, dystrophia"
- Dystrophy, dystrophia
- adiposogenital - E23.6 Other disorders of pituitary gland
- autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker - G71.01 Duchenne or Becker muscular dystrophy
- Becker's type - G71.01 Duchenne or Becker muscular dystrophy
- cervical sympathetic - G90.2 Horner's syndrome
- choroid (hereditary) - H31.20 Hereditary choroidal dystrophy, unspecified
- cornea (hereditary) - H18.50 Unspecified hereditary corneal dystrophies
- endothelial - H18.51 Endothelial corneal dystrophy
- epithelial - H18.52 Epithelial (juvenile) corneal dystrophy
- granular - H18.53 Granular corneal dystrophy
- lattice - H18.54 Lattice corneal dystrophy
- macular - H18.55 Macular corneal dystrophy
- specified type NEC - H18.59 Other hereditary corneal dystrophies
- Duchenne's type - G71.01 Duchenne or Becker muscular dystrophy
- due to malnutrition - E45 Retarded development following protein-calorie malnutrition
- Erb's - G71.02 Facioscapulohumeral muscular dystrophy
- Fuchs' - H18.51 Endothelial corneal dystrophy
- Gower's muscular - G71.01 Duchenne or Becker muscular dystrophy
- hair - L67.8 Other hair color and hair shaft abnormalities
- infantile neuraxonal - G31.89 Other specified degenerative diseases of nervous system
- Landouzy-Déjérine - G71.02 Facioscapulohumeral muscular dystrophy
- Leyden-Möbius - See Also: Dystrophy, muscular, limb-girdle, by type; - G71.039 Limb girdle muscular dystrophy, unspecified
- meaning Limb girdle muscular dystrophy NOS - G71.039 Limb girdle muscular dystrophy, unspecified
- meaning Limb girdle muscular dystrophy type 2A (autosomal recessive) - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- meaning Limb girdle muscular dystrophy, other specified type, - See: by type;
- meaning Limb girdle muscular dystrophy, specified type NEC - G71.038 Other limb girdle muscular dystrophy
- muscular - G71.00 Muscular dystrophy, unspecified
- autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or Becker - G71.01 Duchenne or Becker muscular dystrophy
- benign (Becker type) - G71.01 Duchenne or Becker muscular dystrophy
- scapuloperoneal with early contractures [Emery-Dreifuss] - G71.09 Other specified muscular dystrophies
- congenital (hereditary) (progressive) (with specific morphological abnormalities of the muscle fiber) - G71.09 Other specified muscular dystrophies
- myotonic - G71.11 Myotonic muscular dystrophy
- distal - G71.09 Other specified muscular dystrophies
- Duchenne type - G71.01 Duchenne or Becker muscular dystrophy
- Emery-Dreifuss - G71.09 Other specified muscular dystrophies
- Erb type - G71.02 Facioscapulohumeral muscular dystrophy
- facioscapulohumeral - G71.02 Facioscapulohumeral muscular dystrophy
- Gower's - G71.01 Duchenne or Becker muscular dystrophy
- hereditary (progressive) - See Also: Dystrophy, muscular, by type; - G71.09 Other specified muscular dystrophies
- Landouzy-Déjérine type - G71.02 Facioscapulohumeral muscular dystrophy
- limb-girdle - G71.039 Limb girdle muscular dystrophy, unspecified
- autosomal recessive NEC - G71.038 Other limb girdle muscular dystrophy
- D1 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- D2 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- D3 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- D4 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- D5 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- due to
- alpha sarcoglycan dysfunction - G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- anoctamin-5 dysfunction - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
- beta sarcoglycan dysfunction - G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- sarcoglycan dysfunction, specified NEC - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- R1 (autosomal recessive) - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- R10 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R11 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R12 (autosomal recessive) - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
- R13 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R14 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R15 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R16 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R17 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R18 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R19 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R2 (autosomal recessive) - G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction
- R20 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R21 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R22 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R23 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R24 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R3 (autosomal recessive) - G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- R4 (autosomal recessive) - G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- R5 (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- R6 (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- R7 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R8 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- R9 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- type 1 (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- type 1A (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- type 1B (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- type 1C (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- type 1E (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- type 1H (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- type 1I (autosomal dominant) - G71.031 Autosomal dominant limb girdle muscular dystrophy
- type 2 (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- specified NEC - G71.038 Other limb girdle muscular dystrophy
- type 2A (autosomal recessive) - G71.032 Autosomal recessive limb girdle muscular dystrophy due to calpain-3 dysfunction
- type 2B (autosomal recessive) - G71.033 Limb girdle muscular dystrophy due to dysferlin dysfunction
- type 2C (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- type 2D (autosomal recessive) - G71.0341 Limb girdle muscular dystrophy due to alpha sarcoglycan dysfunction
- type 2E (autosomal recessive) - G71.0342 Limb girdle muscular dystrophy due to beta sarcoglycan dysfunction
- type 2F (autosomal recessive) - G71.0349 Limb girdle muscular dystrophy due to other sarcoglycan dysfunction
- type 2I (autosomal recessive) - G71.038 Other limb girdle muscular dystrophy
- type 2L (autosomal recessive) - G71.035 Limb girdle muscular dystrophy due to anoctamin-5 dysfunction
- myotonic - G71.11 Myotonic muscular dystrophy
- progressive (hereditary) - See Also: Dystrophy, muscular, by type; - G71.09 Other specified muscular dystrophies
- Charcot-Marie (-Tooth) type - G60.0 Hereditary motor and sensory neuropathy
- pseudohypertrophic (infantile) - G71.01 Duchenne or Becker muscular dystrophy
- scapulohumeral - G71.02 Facioscapulohumeral muscular dystrophy
- scapuloperoneal - G71.09 Other specified muscular dystrophies
- severe (Duchenne type) - G71.01 Duchenne or Becker muscular dystrophy
- specified type NEC - G71.09 Other specified muscular dystrophies
- myocardium, myocardial - See: Degeneration, myocardial;
- myotonic, myotonica - G71.11 Myotonic muscular dystrophy
- nail - L60.3 Nail dystrophy
- congenital - Q84.6 Other congenital malformations of nails
- nutritional - E45 Retarded development following protein-calorie malnutrition
- ocular - G71.09 Other specified muscular dystrophies
- oculocerebrorenal - E72.03 Lowe's syndrome
- oculopharyngeal - G71.09 Other specified muscular dystrophies
- ovarian - N83.8 Other noninflammatory disorders of ovary, fallopian tube and broad ligament
- polyglandular - E31.8 Other polyglandular dysfunction
- reflex (neuromuscular) (sympathetic) - See: Syndrome, pain, complex regional I;
- retinal (hereditary) - H35.50 Unspecified hereditary retinal dystrophy
- Salzmann's nodular - See: Degeneration, cornea, nodular;
- scapuloperoneal - G71.09 Other specified muscular dystrophies
- skin NEC - L98.8 Other specified disorders of the skin and subcutaneous tissue
- sympathetic (reflex) - See: Syndrome, pain, complex regional I;
- cervical - G90.2 Horner's syndrome
- tapetoretinal - H35.54 Dystrophies primarily involving the retinal pigment epithelium
- thoracic, asphyxiating - Q77.2 Short rib syndrome
- unguium - L60.3 Nail dystrophy
- congenital - Q84.6 Other congenital malformations of nails
- vitreoretinal - H35.51 Vitreoretinal dystrophy
- vulva - N90.4 Leukoplakia of vulva
- yellow (liver) - See: Failure, hepatic;
Applicable Clinical Terms Definitions
Hair: A filament-like structure consisting of a shaft which projects to the surface of the SKIN from a root which is softer than the shaft and lodges in the cavity of a HAIR FOLLICLE. It is found on most surfaces of the body.
Nails: The thin, horny plates that cover the dorsal surfaces of the distal phalanges of the fingers and toes of primates.
Vulva: The external genitalia of the female. It includes the CLITORIS, the labia, the vestibule, and its glands.