Cataract (cortical) (immature) (incipient)

  • Cataract (cortical) (immature) (incipient) - H26.9 Unspecified cataract
    • anterior
      • and posterior axial embryonal - Q12.0 Congenital cataract
      • pyramidal - Q12.0 Congenital cataract
    • associated with
      • galactosemia - E74.21 Galactosemia
      • myotonic disorders - G71.19 Other specified myotonic disorders
    • blue - Q12.0 Congenital cataract
    • central - Q12.0 Congenital cataract
    • cerulean - Q12.0 Congenital cataract
    • complicated - H26.20 Unspecified complicated cataract
      • glaucomatous flecks - H26.23 Glaucomatous flecks (subcapsular)
      • with
        • neovascularization - H26.21 Cataract with neovascularization
        • ocular disorder - H26.22 Cataract secondary to ocular disorders (degenerative) (inflammatory)
    • congenital - Q12.0 Congenital cataract
    • coraliform - Q12.0 Congenital cataract
    • coronary - Q12.0 Congenital cataract
    • crystalline - Q12.0 Congenital cataract
    • diabetic - See: Diabetes, cataract;
    • drug-induced - H26.3 Drug-induced cataract
    • due to
      • ocular disorder - See: Cataract, complicated;
      • radiation - H26.8 Other specified cataract
    • electric - H26.8 Other specified cataract
    • extraction status - Z98.4 Cataract extraction status
    • glass-blower's - H26.8 Other specified cataract
    • heat ray - H26.8 Other specified cataract
    • heterochromic - See: Cataract, complicated;
    • hypermature - See: Cataract, senile, morgagnian type;
    • in (due to)
      • chronic iridocyclitis - See: Cataract, complicated;
      • diabetes - See: Diabetes, cataract;
      • endocrine disease - E34.9 Endocrine disorder, unspecified
      • eye disease - See: Cataract, complicated;
      • hypoparathyroidism - E20.9 Hypoparathyroidism, unspecified
      • malnutrition-dehydration - E46 Unspecified protein-calorie malnutrition
      • metabolic disease - E88.9 Metabolic disorder, unspecified
      • myotonic disorders - G71.19 Other specified myotonic disorders
      • nutritional disease - E63.9 Nutritional deficiency, unspecified
    • infantile - See: Cataract, presenile;
    • irradiational - See: Cataract, specified NEC;
    • juvenile - See: Cataract, presenile;
    • malnutrition-dehydration - E46 Unspecified protein-calorie malnutrition
    • morgagnian - See: Cataract, senile, morgagnian type;
    • myotonic - G71.19 Other specified myotonic disorders
    • myxedema - E03.9 Hypothyroidism, unspecified
    • nuclear
      • embryonal - Q12.0 Congenital cataract
      • sclerosis - See: Cataract, senile, nuclear;
    • presenile - H26.00 Unspecified infantile and juvenile cataract
      • combined forms - H26.06 Combined forms of infantile and juvenile cataract
      • cortical - H26.01 Infantile and juvenile cortical, lamellar, or zonular cataract
      • lamellar - See: Cataract, presenile, cortical;
      • nuclear - H26.03 Infantile and juvenile nuclear cataract
      • specified NEC - H26.09 Other infantile and juvenile cataract
      • subcapsular polar (anterior) - H26.04 Anterior subcapsular polar infantile and juvenile cataract
        • posterior - H26.05 Posterior subcapsular polar infantile and juvenile cataract
      • zonular - See: Cataract, presenile, cortical;
    • secondary - H26.40 Unspecified secondary cataract
      • Soemmering's ring - H26.41 Soemmering's ring
      • specified NEC - H26.49 Other secondary cataract
      • to eye disease - See: Cataract, complicated;
    • senile - H25.9 Unspecified age-related cataract
      • brunescens - See: Cataract, senile, nuclear;
      • combined forms - H25.81 Combined forms of age-related cataract
      • coronary - See: Cataract, senile, incipient;
      • cortical - H25.01 Cortical age-related cataract
      • hypermature - See: Cataract, senile, morgagnian type;
      • incipient (mature) (total) - H25.09 Other age-related incipient cataract
        • cortical - See: Cataract, senile, cortical;
        • subcapsular - See: Cataract, senile, subcapsular;
      • morgagnian type (hypermature) - H25.2 Age-related cataract, morgagnian type
      • nuclear (sclerosis) - H25.1 Age-related nuclear cataract
      • polar subcapsular (anterior) (posterior) - See: Cataract, senile, incipient;
      • punctate - See: Cataract, senile, incipient;
      • specified NEC - H25.89 Other age-related cataract
      • subcapsular polar (anterior) - H25.03 Anterior subcapsular polar age-related cataract
        • posterior - H25.04 Posterior subcapsular polar age-related cataract
    • snowflake - See: Diabetes, cataract;
    • specified NEC - H26.8 Other specified cataract
    • toxic - See: Cataract, drug-induced;
    • traumatic - H26.10 Unspecified traumatic cataract
      • localized - H26.11 Localized traumatic opacities
      • partially resolved - H26.12 Partially resolved traumatic cataract
      • total - H26.13 Total traumatic cataract
    • with
      • neovascularization - See: Cataract, complicated;
    • zonular (perinuclear) - Q12.0 Congenital cataract

Footnotes

Endocrine System Diseases: Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES.

Eye Diseases: Diseases affecting the eye.

Galactosemias: A group of inherited enzyme deficiencies which feature elevations of GALACTOSE in the blood. This condition may be associated with deficiencies of GALACTOKINASE; UDPGLUCOSE-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE; or UDPGLUCOSE 4-EPIMERASE. The classic form is caused by UDPglucose-Hexose-1-Phosphate Uridylyltransferase deficiency, and presents in infancy with FAILURE TO THRIVE; VOMITING; and INTRACRANIAL HYPERTENSION. Affected individuals also may develop MENTAL RETARDATION; JAUNDICE; hepatosplenomegaly; ovarian failure (PRIMARY OVARIAN INSUFFICIENCY); and cataracts. (From Menkes, Textbook of Child Neurology, 5th ed, pp61-3)

Hypoparathyroidism: A condition caused by a deficiency of PARATHYROID HORMONE (or PTH). It is characterized by HYPOCALCEMIA and hyperphosphatemia. Hypocalcemia leads to TETANY. The acquired form is due to removal or injuries to the PARATHYROID GLANDS. The congenital form is due to mutations of genes, such as TBX1; (see DIGEORGE SYNDROME); CASR encoding CALCIUM-SENSING RECEPTOR; or PTH encoding parathyroid hormone.

Metabolic Diseases: Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed)

Myotonic Disorders: Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition.

Myxedema: A condition characterized by a dry, waxy type of swelling (EDEMA) with abnormal deposits of MUCOPOLYSACCHARIDES in the SKIN and other tissues. It is caused by a deficiency of THYROID HORMONES. The skin becomes puffy around the eyes and on the cheeks. The face is dull and expressionless with thickened nose and lips.

Radiation: Emission or propagation of acoustic waves (SOUND), ELECTROMAGNETIC ENERGY waves (such as LIGHT; RADIO WAVES; GAMMA RAYS; or X-RAYS), or a stream of subatomic particles (such as ELECTRONS; NEUTRONS; PROTONS; or ALPHA PARTICLES).

Sclerosis: A pathological process consisting of hardening or fibrosis of an anatomical structure, often a vessel or a nerve.

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