• Aplasia - see also Agenesis

    • abdominal muscle syndrome Q79.4
      ICD-10-CM Diagnosis Code Q79.4

      Prune belly syndrome

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital prolapse of bladder mucosa
      • Eagle-Barrett syndrome
    • alveolar process (acquired) - see Anomaly, alveolar
      • congenital Q38.6
        ICD-10-CM Diagnosis Code Q38.6

        Other congenital malformations of mouth

          2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
        Applicable To
        • Congenital malformation of mouth NOS
    • aorta Q25.41
      (congenital)
      ICD-10-CM Diagnosis Code Q25.41

      Absence and aplasia of aorta

        2017 - New Code 2018 2019 2020 Billable/Specific Code POA Exempt
    • axialis extracorticalis E75.29
      (congenita)
      ICD-10-CM Diagnosis Code E75.29

      Other sphingolipidosis

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Farber's syndrome
      • Sulfatide lipidosis
    • bone marrow (myeloid) D61.9
      ICD-10-CM Diagnosis Code D61.9

      Aplastic anemia, unspecified

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Hypoplastic anemia NOS
      • Medullary hypoplasia
      • congenital D61.01
        ICD-10-CM Diagnosis Code D61.01

        Constitutional (pure) red blood cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
        Applicable To
        • Blackfan-Diamond syndrome
        • Congenital (pure) red cell aplasia
        • Familial hypoplastic anemia
        • Primary (pure) red cell aplasia
        • Red cell (pure) aplasia of infants
        Type 1 Excludes
        • acquired red cell aplasia (D60.9)
    • brain Q00.0
      ICD-10-CM Diagnosis Code Q00.0

      Anencephaly

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Acephaly
      • Acrania
      • Amyelencephaly
      • Hemianencephaly
      • Hemicephaly
      • part of Q04.3
        ICD-10-CM Diagnosis Code Q04.3

        Other reduction deformities of brain

          2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
        Applicable To
        • Absence of part of brain
        • Agenesis of part of brain
        • Agyria
        • Aplasia of part of brain
        • Hydranencephaly
        • Hypoplasia of part of brain
        • Lissencephaly
        • Microgyria
        • Pachygyria
        Type 1 Excludes
        • congenital malformations of corpus callosum (Q04.0)
    • bronchus Q32.4
      ICD-10-CM Diagnosis Code Q32.4

      Other congenital malformations of bronchus

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Absence of bronchus
      • Agenesis of bronchus
      • Atresia of bronchus
      • Congenital diverticulum of bronchus
      • Congenital malformation of bronchus NOS
    • cementum K00.4
      ICD-10-CM Diagnosis Code K00.4

      Disturbances in tooth formation

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Aplasia and hypoplasia of cementum
      • Dilaceration of tooth
      • Enamel hypoplasia (neonatal) (postnatal) (prenatal)
      • Regional odontodysplasia
      • Turner's tooth
      Type 1 Excludes
      • Hutchinson's teeth and mulberry molars in congenital syphilis (A50.5)
      Type 2 Excludes
    • cerebellum Q04.3
      ICD-10-CM Diagnosis Code Q04.3

      Other reduction deformities of brain

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Absence of part of brain
      • Agenesis of part of brain
      • Agyria
      • Aplasia of part of brain
      • Hydranencephaly
      • Hypoplasia of part of brain
      • Lissencephaly
      • Microgyria
      • Pachygyria
      Type 1 Excludes
      • congenital malformations of corpus callosum (Q04.0)
    • cervix Q51.5
      (congenital)
      ICD-10-CM Diagnosis Code Q51.5

      Agenesis and aplasia of cervix

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital absence of cervix
    • congenital pure red cell D61.01
      ICD-10-CM Diagnosis Code D61.01

      Constitutional (pure) red blood cell aplasia

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Blackfan-Diamond syndrome
      • Congenital (pure) red cell aplasia
      • Familial hypoplastic anemia
      • Primary (pure) red cell aplasia
      • Red cell (pure) aplasia of infants
      Type 1 Excludes
      • acquired red cell aplasia (D60.9)
    • corpus callosum Q04.0
      ICD-10-CM Diagnosis Code Q04.0

      Congenital malformations of corpus callosum

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Agenesis of corpus callosum
    • cutis congenita Q84.8
      ICD-10-CM Diagnosis Code Q84.8

      Other specified congenital malformations of integument

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Aplasia cutis congenita
    • erythrocyte congenital D61.01
      ICD-10-CM Diagnosis Code D61.01

      Constitutional (pure) red blood cell aplasia

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Blackfan-Diamond syndrome
      • Congenital (pure) red cell aplasia
      • Familial hypoplastic anemia
      • Primary (pure) red cell aplasia
      • Red cell (pure) aplasia of infants
      Type 1 Excludes
      • acquired red cell aplasia (D60.9)
    • extracortical axial E75.29
      ICD-10-CM Diagnosis Code E75.29

      Other sphingolipidosis

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Farber's syndrome
      • Sulfatide lipidosis
    • eye Q11.1
      ICD-10-CM Diagnosis Code Q11.1

      Other anophthalmos

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Anophthalmos NOS
      • Agenesis of eye
      • Aplasia of eye
    • fovea centralis Q14.1
      (congenital)
      ICD-10-CM Diagnosis Code Q14.1

      Congenital malformation of retina

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital retinal aneurysm
    • gallbladder, congenital Q44.0
      ICD-10-CM Diagnosis Code Q44.0

      Agenesis, aplasia and hypoplasia of gallbladder

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital absence of gallbladder
    • iris Q13.1
      ICD-10-CM Diagnosis Code Q13.1

      Absence of iris

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Aniridia
      Use Additional
      • code for associated glaucoma (H42)
    • labyrinth, membranous Q16.5
      ICD-10-CM Diagnosis Code Q16.5

      Congenital malformation of inner ear

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital anomaly of membranous labyrinth
      • Congenital anomaly of organ of Corti
    • limb (congenital) Q73.8
      ICD-10-CM Diagnosis Code Q73.8

      Other reduction defects of unspecified limb(s)

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Longitudinal reduction deformity of unspecified limb(s)
      • Ectromelia of limb NOS
      • Hemimelia of limb NOS
      • Reduction defect of limb NOS
    • lung, congenital Q33.3
      (bilateral) (unilateral)
      ICD-10-CM Diagnosis Code Q33.3

      Agenesis of lung

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital absence of lung (lobe)
    • pancreas Q45.0
      ICD-10-CM Diagnosis Code Q45.0

      Agenesis, aplasia and hypoplasia of pancreas

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital absence of pancreas
    • parathyroid-thymic D82.1
      ICD-10-CM Diagnosis Code D82.1

      Di George's syndrome

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Pharyngeal pouch syndrome
      • Thymic alymphoplasia
      • Thymic aplasia or hypoplasia with immunodeficiency
    • Pelizaeus-Merzbacher E75.29
      ICD-10-CM Diagnosis Code E75.29

      Other sphingolipidosis

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Farber's syndrome
      • Sulfatide lipidosis
    • penis Q55.5
      ICD-10-CM Diagnosis Code Q55.5

      Congenital absence and aplasia of penis

        2016 2017 2018 2019 2020 Billable/Specific Code Male Dx POA Exempt
    • prostate Q55.4
      ICD-10-CM Diagnosis Code Q55.4

      Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate

        2016 2017 2018 2019 2020 Billable/Specific Code Male Dx POA Exempt
      Applicable To
      • Absence or aplasia of prostate
      • Absence or aplasia of spermatic cord
      • Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS
    • red cell (with thymoma) D60.9
      ICD-10-CM Diagnosis Code D60.9

      Acquired pure red cell aplasia, unspecified

        2016 2017 2018 2019 2020 Billable/Specific Code
      • acquired D60.9
        ICD-10-CM Diagnosis Code D60.9

        Acquired pure red cell aplasia, unspecified

          2016 2017 2018 2019 2020 Billable/Specific Code
        • due to drugs D60.9
          ICD-10-CM Diagnosis Code D60.9

          Acquired pure red cell aplasia, unspecified

            2016 2017 2018 2019 2020 Billable/Specific Code
      • adult D60.9
        ICD-10-CM Diagnosis Code D60.9

        Acquired pure red cell aplasia, unspecified

          2016 2017 2018 2019 2020 Billable/Specific Code
      • chronic D60.0
        ICD-10-CM Diagnosis Code D60.0

        Chronic acquired pure red cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
      • congenital D61.01
        ICD-10-CM Diagnosis Code D61.01

        Constitutional (pure) red blood cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
        Applicable To
        • Blackfan-Diamond syndrome
        • Congenital (pure) red cell aplasia
        • Familial hypoplastic anemia
        • Primary (pure) red cell aplasia
        • Red cell (pure) aplasia of infants
        Type 1 Excludes
        • acquired red cell aplasia (D60.9)
      • constitutional D61.01
        ICD-10-CM Diagnosis Code D61.01

        Constitutional (pure) red blood cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
        Applicable To
        • Blackfan-Diamond syndrome
        • Congenital (pure) red cell aplasia
        • Familial hypoplastic anemia
        • Primary (pure) red cell aplasia
        • Red cell (pure) aplasia of infants
        Type 1 Excludes
        • acquired red cell aplasia (D60.9)
      • due to drugs D60.9
        ICD-10-CM Diagnosis Code D60.9

        Acquired pure red cell aplasia, unspecified

          2016 2017 2018 2019 2020 Billable/Specific Code
      • hereditary D61.01
        ICD-10-CM Diagnosis Code D61.01

        Constitutional (pure) red blood cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
        Applicable To
        • Blackfan-Diamond syndrome
        • Congenital (pure) red cell aplasia
        • Familial hypoplastic anemia
        • Primary (pure) red cell aplasia
        • Red cell (pure) aplasia of infants
        Type 1 Excludes
        • acquired red cell aplasia (D60.9)
      • of infants D61.01
        ICD-10-CM Diagnosis Code D61.01

        Constitutional (pure) red blood cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
        Applicable To
        • Blackfan-Diamond syndrome
        • Congenital (pure) red cell aplasia
        • Familial hypoplastic anemia
        • Primary (pure) red cell aplasia
        • Red cell (pure) aplasia of infants
        Type 1 Excludes
        • acquired red cell aplasia (D60.9)
      • primary D61.01
        ICD-10-CM Diagnosis Code D61.01

        Constitutional (pure) red blood cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
        Applicable To
        • Blackfan-Diamond syndrome
        • Congenital (pure) red cell aplasia
        • Familial hypoplastic anemia
        • Primary (pure) red cell aplasia
        • Red cell (pure) aplasia of infants
        Type 1 Excludes
        • acquired red cell aplasia (D60.9)
      • pure D61.01
        ICD-10-CM Diagnosis Code D61.01

        Constitutional (pure) red blood cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
        Applicable To
        • Blackfan-Diamond syndrome
        • Congenital (pure) red cell aplasia
        • Familial hypoplastic anemia
        • Primary (pure) red cell aplasia
        • Red cell (pure) aplasia of infants
        Type 1 Excludes
        • acquired red cell aplasia (D60.9)
        • due to drugs D60.9
          ICD-10-CM Diagnosis Code D60.9

          Acquired pure red cell aplasia, unspecified

            2016 2017 2018 2019 2020 Billable/Specific Code
      • specified type NEC D60.8
        ICD-10-CM Diagnosis Code D60.8

        Other acquired pure red cell aplasias

          2016 2017 2018 2019 2020 Billable/Specific Code
      • transient D60.1
        ICD-10-CM Diagnosis Code D60.1

        Transient acquired pure red cell aplasia

          2016 2017 2018 2019 2020 Billable/Specific Code
    • round ligament Q52.8
      ICD-10-CM Diagnosis Code Q52.8

      Other specified congenital malformations of female genitalia

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    • skin Q84.8
      ICD-10-CM Diagnosis Code Q84.8

      Other specified congenital malformations of integument

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Aplasia cutis congenita
    • spermatic cord Q55.4
      ICD-10-CM Diagnosis Code Q55.4

      Other congenital malformations of vas deferens, epididymis, seminal vesicles and prostate

        2016 2017 2018 2019 2020 Billable/Specific Code Male Dx POA Exempt
      Applicable To
      • Absence or aplasia of prostate
      • Absence or aplasia of spermatic cord
      • Congenital malformation of vas deferens, epididymis, seminal vesicles or prostate NOS
    • spleen Q89.01
      ICD-10-CM Diagnosis Code Q89.01

      Asplenia (congenital)

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
    • testicle Q55.0
      ICD-10-CM Diagnosis Code Q55.0

      Absence and aplasia of testis

        2016 2017 2018 2019 2020 Billable/Specific Code Male Dx POA Exempt
      Applicable To
      • Monorchism
    • thymic, with immunodeficiency D82.1
      ICD-10-CM Diagnosis Code D82.1

      Di George's syndrome

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Pharyngeal pouch syndrome
      • Thymic alymphoplasia
      • Thymic aplasia or hypoplasia with immunodeficiency
    • thyroid E03.1
      (congenital) (with myxedema)
      ICD-10-CM Diagnosis Code E03.1

      Congenital hypothyroidism without goiter

        2016 2017 2018 2019 2020 Billable/Specific Code
      Applicable To
      • Aplasia of thyroid (with myxedema)
      • Congenital atrophy of thyroid
      • Congenital hypothyroidism NOS
    • uterus Q51.0
      ICD-10-CM Diagnosis Code Q51.0

      Agenesis and aplasia of uterus

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Congenital absence of uterus
    • ventral horn cell Q06.1
      ICD-10-CM Diagnosis Code Q06.1

      Hypoplasia and dysplasia of spinal cord

        2016 2017 2018 2019 2020 Billable/Specific Code POA Exempt
      Applicable To
      • Atelomyelia
      • Myelatelia
      • Myelodysplasia of spinal cord