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2008 ICD-9-CM Diagnosis Code 742
Other congenital anomalies of nervous system
2008 ICD-9-CM Diagnosis Code 742.1
Microcephalus
  • abnormal smallness of the brain.
  • Smallness of the head produced by incomplete development of the brain, often associated with below normal mental and cognitive development.
2008 ICD-9-CM Diagnosis Code 742.2
Congenital reduction deformities of brain
2008 ICD-9-CM Diagnosis Code 742.3
Congenital hydrocephalus
  • Hydrocephalus, absence of the cerebellar vermis, and posterior fossa cyst continuous with the fourth ventricle are the main characteristics of this syndrome. About 4% of all cases of hydrocephalus are complicated by DWS. Associated disorders may include Aase-Smith syndrome 1, Aicardi, Coffin-Siris, cryptophthalmos, Ehlers-Danlos, Ellis-van Creveld, Jones syndrome, Joubert, Ruvalcaba-Myhre-Smith, Walker-Warburg, Meckel, Ritscher-Schinzel, and Veradi syndromes. Dandy-Walker syndrome associated with macrocephaly, facial anomalies, developmental delay, and brain stem dysgenesis inherited as an X-linked recessive trait was reported as a separate syndrome.
2008 ICD-9-CM Diagnosis Code 742.4
Other specified congenital anomalies of brain
2008 ICD-9-CM Diagnosis Code 742.5
Other specified congenital anomalies of spinal cord
2008 ICD-9-CM Diagnosis Code 742.59
Other specified congenital anomalies of spinal cord
2008 ICD-9-CM Diagnosis Code 742.8
Other specified congenital anomalies of nervous system
  • autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent; clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension, fixed pupils, excessive sweating, loss of pain and temperature sensation, and absent reflexes; pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons.
2008 ICD-9-CM Diagnosis Code 742.9
Unspecified congenital anomaly of brain spinal cord and nervous system
  • structural or functional abnormalities of the central or peripheral nervous system existing at birth and often before birth, resulting primarily from defects of embryogenesis.
  • pathologic condition existing at, and usually before, birth affecting the brain, which is composed of the intracranial components of the central nervous system.