Aplasia
- See see also Agenesis
- abdominal muscle syndromeQ79.4
- alveolar process (acquired)See Anomaly, alveolar
- alveolar process (acquired), congenitalQ38.6
- aorta (congenital)Q25.41
- axialis extracorticalis (congenita)E75.29
- bone marrow (myeloid)D61.9
- bone marrow (myeloid), congenitalD61.01
- brainQ00.0
- brain, part ofQ04.3
- bronchusQ32.4
- cementumK00.4
- cerebellumQ04.3
- cervix (congenital)Q51.5
- congenital pure red cellD61.01
- corpus callosumQ04.0
- cutis congenitaQ84.8
- erythrocyte congenitalD61.01
- extracortical axialE75.29
- eyeQ11.1
- fovea centralis (congenital)Q14.1
- gallbladder, congenitalQ44.0
- irisQ13.1
- labyrinth, membranousQ16.5
- limb (congenital)Q73.8
- limb (congenital), lowerSee Defect, reduction, lower limb
- limb (congenital), upperSee Agenesis, arm
- lung, congenital (bilateral) (unilateral)Q33.3
- pancreasQ45.0
- parathyroid-thymicD82.1
- Pelizaeus-MerzbacherE75.27
- penisQ55.5
- prostateQ55.4
- red cell (with thymoma)D60.9
- red cell (with thymoma), acquiredD60.9
- red cell (with thymoma), acquired, due to drugsD60.9
- red cell (with thymoma), adultD60.9
- red cell (with thymoma), chronicD60.0
- red cell (with thymoma), congenitalD61.01
- red cell (with thymoma), constitutionalD61.01
- red cell (with thymoma), due to drugsD60.9
- red cell (with thymoma), hereditaryD61.01
- red cell (with thymoma), of infantsD61.01
- red cell (with thymoma), primaryD61.01
- red cell (with thymoma), pureD61.01
- red cell (with thymoma), pure, due to drugsD60.9
- red cell (with thymoma), specified type NECD60.8
- red cell (with thymoma), transientD60.1
- round ligamentQ52.8
- skinQ84.8
- spermatic cordQ55.4
- spleenQ89.01
- testicleQ55.0
- thymic, with immunodeficiencyD82.1
- thyroid (congenital) (with myxedema)E03.1
- uterusQ51.0
- ventral horn cellQ06.1