Aplasia

"Aplasia" 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 "aplasia"

  • Aplasia - See Also: Agenesis;
    • abdominal muscle syndrome - Q79.4 Prune belly syndrome
    • alveolar process (acquired) - See: Anomaly, alveolar;
      • congenital - Q38.6 Other congenital malformations of mouth
    • aorta (congenital) - Q25.41 Absence and aplasia of aorta
    • axialis extracorticalis (congenita) - E75.29 Other sphingolipidosis
    • bone marrow (myeloid) - D61.9 Aplastic anemia, unspecified
      • congenital - D61.01 Constitutional (pure) red blood cell aplasia
    • brain - Q00.0 Anencephaly
      • part of - Q04.3 Other reduction deformities of brain
    • bronchus - Q32.4 Other congenital malformations of bronchus
    • cementum - K00.4 Disturbances in tooth formation
    • cerebellum - Q04.3 Other reduction deformities of brain
    • cervix (congenital) - Q51.5 Agenesis and aplasia of cervix
    • congenital pure red cell - D61.01 Constitutional (pure) red blood cell aplasia
    • corpus callosum - Q04.0 Congenital malformations of corpus callosum
    • cutis congenita - Q84.8 Other specified congenital malformations of integument
    • erythrocyte congenital - D61.01 Constitutional (pure) red blood cell aplasia
    • extracortical axial - E75.29 Other sphingolipidosis
    • eye - Q11.1 Other anophthalmos
    • fovea centralis (congenital) - Q14.1 Congenital malformation of retina
    • gallbladder, congenital - Q44.0 Agenesis, aplasia and hypoplasia of gallbladder
    • iris - Q13.1 Absence of iris
    • labyrinth, membranous - Q16.5 Congenital malformation of inner ear
    • limb (congenital) - Q73.8 Other reduction defects of unspecified limb(s)
      • lower - See: Defect, reduction, lower limb;
      • upper - See: Agenesis, arm;
    • lung, congenital (bilateral) (unilateral) - Q33.3 Agenesis of lung
    • pancreas - Q45.0 Agenesis, aplasia and hypoplasia of pancreas
    • parathyroid-thymic - D82.1 Di George's syndrome
    • Pelizaeus-Merzbacher - E75.29 Other sphingolipidosis
    • penis - Q55.5 Congenital absence and aplasia of penis
    • prostate - Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
    • red cell (with thymoma) - D60.9 Acquired pure red cell aplasia, unspecified
      • acquired - D60.9 Acquired pure red cell aplasia, unspecified
        • due to drugs - D60.9 Acquired pure red cell aplasia, unspecified
      • adult - D60.9 Acquired pure red cell aplasia, unspecified
      • chronic - D60.0 Chronic acquired pure red cell aplasia
      • congenital - D61.01 Constitutional (pure) red blood cell aplasia
      • constitutional - D61.01 Constitutional (pure) red blood cell aplasia
      • due to drugs - D60.9 Acquired pure red cell aplasia, unspecified
      • hereditary - D61.01 Constitutional (pure) red blood cell aplasia
      • of infants - D61.01 Constitutional (pure) red blood cell aplasia
      • primary - D61.01 Constitutional (pure) red blood cell aplasia
      • pure - D61.01 Constitutional (pure) red blood cell aplasia
        • due to drugs - D60.9 Acquired pure red cell aplasia, unspecified
      • specified type NEC - D60.8 Other acquired pure red cell aplasias
      • transient - D60.1 Transient acquired pure red cell aplasia
    • round ligament - Q52.8 Other specified congenital malformations of female genitalia
    • skin - Q84.8 Other specified congenital malformations of integument
    • spermatic cord - Q55.4 Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate
    • spleen - Q89.01 Asplenia (congenital)
    • testicle - Q55.0 Absence and aplasia of testis
    • thymic, with immunodeficiency - D82.1 Di George's syndrome
    • thyroid (congenital) (with myxedema) - E03.1 Congenital hypothyroidism without goiter
    • uterus - Q51.0 Agenesis and aplasia of uterus
    • ventral horn cell - Q06.1 Hypoplasia and dysplasia of spinal cord