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2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Congential Anomalies 740-759 > Other Congenital Anomalies Of Nervous System 742.* > 2008 ICD-9-CM Diagnosis 742.0 Encephalocele Cerebral tissue herniation through a congenital or acquired defect in the skull. The majority of congenital encephaloceles occur in the occipital or frontal regions. Clinical features include a protuberant mass that may be pulsatile. The quantity and location of protruding neural tissue determines the type and degree of neurologic deficit. Visual defects, psychomotor developmental delay, and persistent motor deficits frequently occur. 742.0 is a specific code that can be used to specify a diagnosis 742.0 contains 35 index entries View the ICD-9-CM Volume 1 742.* hierarchy 742.0 also known as: Encephalocystocele Encephalomyelocele Hydroencephalocele Hydromeningocele, cranial Meningocele, cerebral Meningoencephalocele Index entries containing 742.0: Absence (organ or part) (complete or partial) roof of orbit (congenital) 742.0 skull bone 756.0 with encephalocele 742.0 Agenesis - see also Absence, by site, congenital roof of orbit 742.0 skull (bone) 756.0 with encephalocele 742.0 Anomaly, anomalous (congenital) (unspecified type) 759.9 bone NEC 756.9 skull 756.0 with encephalocele 742.0 skull (bone) 756.0 with encephalocele 742.0 specified type NEC bone(s) 756.9 skull 756.0 with encephalocele 742.0 skull (bone(s)) 756.0 with encephalocele 742.0 Arnold-Chiari obstruction or syndrome (see also Spina bifida) 741.0 type III 742.0 Cephalocele 742.0 Chiari's malformation type III 742.0 Deformity 738.9 skull (acquired) 738.19 congenital 756.0 with encephalocele 742.0 Distortion (congenital) skull bone(s) 756.0 with encephalocele 742.0 Encephalocele 742.0 orbit 376.81 Encephalocystocele 742.0 Encephalomeningocele 742.0 Encephalomyelocele 742.0 Exencephalus, exencephaly 742.0 Hernia, hernial (acquired) (recurrent) 553.9 brain 348.4 congenital 742.0 cerebral 348.4 congenital 742.0 endaural 742.0 Hydrencephalocele (congenital) 742.0 Hydrencephalomeningocele (congenital) 742.0 Hydroencephalocele (congenital) 742.0 Hydroencephalomeningocele (congenital) 742.0 Hydromeningocele (spinal) (see also Spina bifida) 741.9 cranial 742.0 Hypoplasia, hypoplasis 759.89 skull (bone) 756.0 with encephalocele 742.0 Imperfect closure (congenital) roof of orbit 742.0 skull 756.0 with encephalocele 742.0 Malformation (congenital) - see also Anomaly Chiari type III 742.0 Meningocele (congenital) (spinal) (see also Spina bifida) 741.9 cerebral 742.0 cranial 742.0 Meningoencephalocele 742.0 syphilitic 094.89 congenital 090.49 Sinus - see also Fistula pericranii 742.0 Syndrome - see also Disease Arnold-Chiari (see also Spina bifida) 741.0 type III 742.0