This page provides the full title for the ICD diagnosis code "Q04.4 Septo-optic dysplasia" and its subcategories. ICD-10-CM/PCS MS-DRG v35.0 Definitions Manual: Skip to content: Appendix C: Principal diagnoses which convert CC/MCC to non-CC: Page 195 of 313 : . Index to Diseases and Injuries Bronchopulmonary dysplasia originating in the perinatal period: P278: MCC: . The most common features are underdevelopment (hypoplasia) of the eye (optic) nerve, abnormal formation of structures along the midline of the brain such as the absence of the septum pellucidum and the corpus callosum, and a small pituitary (pituitary hypoplasia). Dysplasia see also Anomaly.

BILLABLE Q04.4 Septo-optic dysplasia of brain ; BILLABLE Q04.5 Megalencephaly ; BILLABLE Q04.6 Congenital cerebral cysts ; . SOD is a condition that can involve multiple problems in the midline .

Rare familial recurrence has been reported, suggesting at least one genetic form .

Code Type-1 Excludes: Type-1 Excludes Type-1 Excludes mean the conditions excluded are mutually exclusive and should never be coded .

acetabular, congenital Q65.89; alveolar capillary, . The phenotype of SOD is highly heterogeneous, and the existence of at least two features is considered sufficient for diagnosis. From Wikipedia, the free encyclopedia Septo-optic dysplasia ( SOD ), known also as de Morsier syndrome, is a rare congenital malformation syndrome that features a combination of the underdevelopment of the optic nerve, pituitary gland dysfunction, and absence of the septum pellucidum (a midline part of the brain).

. Septo-optic dysplasia spectrum. ICD-10-CM Section Q00-Q07 Congenital malformations of the nervous system. 741.93 Spina bifida without hydrocephalus, lumbar region Q05.7 Lumbar spina bifida without hydrocephalus 742.0 Encephalocele Q01.0 Frontal .

vidual domains of the ICD-10 criteria for the diagnosis of aut-ism)12 by an independent clinical researcher who was not part of the clinical team.

This page contains information about ICD-10 code: Q04.Diagnosis. Q04.4 Septo-optic dysplasia Q04.5 Megalencephaly Q04.6 Congenital cerebral cysts Porencephaly Schizencephaly Excludes: acquired porencephalic cysts (G93.0) Q04.60 Multiple congenital cerebral cysts Q04.61 Single congenital cerebral cyst Q04.8 Other specified congenital malformations of brain Macrogyria Walnut brain

Q04.4 Septo-optic dysplasia of brain Q04.5 Megalencephaly Q04.6 Congenital cerebral cysts Inclusion term(s): Porencephaly; Schizencephaly; Q04.5 - Megalencephaly.

Q042: Holoprosencephaly: Q043: Other reduction deformities of brain: Q044: Septo-optic dysplasia of brain: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: Other specified congenital malformations of brain . Q04.4 Septo-optic dysplasia of brain 742.3 Congenital hydrocephalus Q03.0 Malformations of aqueduct of Sylvius Q03.1 Atresia of foramina of Magendie and Luschka Versions. At approximately 12 weeks' gestation, the mother took 60 acetaminophen capsules in a failed suicide attempt. Common clinical features of this malformation include epilepsy, motor deficits, and psychomotor retardation. septo-optic dysplasia 1 approved drug hierarchy tree view. A 'billable code' is detailed enough to be used to specify a medical diagnosis. ICD-9. ICD-10: Q14.2: ICD . Currarino syndrome is an inherited congenital disorder where either the sacrum (the fused vertebrae forming the back of the pelvis) is not formed properly, or there is a mass in the presacral space in front of the sacrum, and there are malformations of the anus or rectum.It occurs in approximately 1 in 100,000 people. BILLABLE Q06.1 Hypoplasia and dysplasia of spinal cord ; BILLABLE Q06.2 Diastematomyelia ; Eye Malformations Q11-Q14, H47 Cystic eyeball Q11.0 Other anophthalmos Q11.1 ICD-10: Q04.4; OMIM: 182230; UMLS: C0162809 C0338503; MeSH: D025962; GARD: 7627; MedDRA: 10067159; Summary ICD-10-CM Q04.4 - Septo-optic dysplasia of brain Code Q04.4 - Septo-optic dysplasia of brain [Billable] [POA Exempt] There's more to see -- the rest of this entry is available only to subscribers. Luokitus . [5] Genetic.

ICD-10-CM Diagnosis Codes; . UMLS C0338503 . (Q 044) Septo-optic dysplasia (Q 045) Megalencephaly (Q 046) Congenital cerebral cysts. septo-optic Q04.4; skin L98.8; spinal cord Q06.1; spondyloepiphyseal Q77.7; thymic, with immunodeficiency D82.1; . Q04.4 is a valid billable ICD-10 diagnosis code for Septo-optic dysplasia of brain . 8 Skeletal Dysplasia ICD-10-CM Coding Rules All fetal anomaly codes begin with a maternal code followed by a fetal code. Schizencephaly (from Greek skhizein 'to split', and enkephalos 'brain') is a rare birth defect characterized by abnormal clefts lined with grey matter that form the ependyma of the cerebral ventricles to the pia mater.These clefts can occur bilaterally or unilaterally. Congenital malformations .

Septo-optic dysplasia of brain HTML | TXT | ICD-10 ⇄ ICD-9 CROSSWALK Q049 (Diagnosis) Congenital malformation of brain, unspecified . Disease definition Septooptic dysplasia (SOD) is a clinically heterogeneous disorder characterized by the classical triad of optic nerve hypoplasia, pituitary hormone abnormalities and midline brain defects.

Select the associated ICD-10 code to view any special notations from the Tabular List. Other specified congenital malformations of brain .

Septo-optic nerve dysplasia is a rare congenital anomaly with optic nerve hypoplasia, pituitary hormone deficiencies and midline developmental defects of the brain. 741.93 Spina bifida without hydrocephalus, lumbar region Q05.7 Lumbar spina bifida without hydrocephalus 742.0 Encephalocele Q01.0 Frontal . .

Septo-optic dysplasia is a disorder of early brain and eye development. Although its signs and symptoms vary, this condition is traditionally defined by three characteristic features: underdevelopment (hypoplasia) of the optic nerves, abnormal formation of structures along the midline of the brain, and pituitary hypoplasia.

Septo -optic dysplasia of brain Q04.4 Congenital cerebral cyst (porencephaly, schizencephaly) Q04.6 . ICD-10-CM/PCS MS-DRG v38.1 Definitions Manual: Skip to content: MDC 01 Diseases and disorders of the nervous system: Assignment of Diagnosis Codes: .

ICD-10 code Q04 for Other congenital malformations of brain is a medical classification as listed by WHO under the range - Congenital malformations, deformations and chromosomal abnormalities .

. Septo-optic dysplasia of brain ICD-10-CM Diagnosis Code S06.2X Diffuse traumatic brain injury ICD-10-PCS Procedure Code 3E0Q Cranial Cavity and Brain ICD-10-PCS Procedure Code 3E1Q Cranial Cavity and Brain ICD-10-PCS Procedure Code D020HZZ [convert to ICD-9-CM] Stereotactic Particulate Radiosurgery of Brain The ICD-10 Code Q04 is assigned to Diagnosis "Other congenital malformations of brain". This code description may also have Includes, Excludes, Notes, Guidelines, Examples and other information. Q04.8.

Children . ICD-10-CM/PCS MS-DRGv33 Definitions Manual: Appendix C Part 1: CC/MCC Codes: Page 16 of 44: . ICD-10-CM/PCS MS-DRGv33 Definitions Manual: MDC 1 Assignment of Diagnosis Codes: .

. MeSH D025962. children with optic nerve hypoplasia (ONH) and or septo-optic dysplasia (SOD),and toinvestigate the relationship between visual impairment, SCRR difculties, ASD, and cognition.

. The ICD-10-CM Alphabetical Index is designed to allow medical coders to look up various medical terms and connect them with the appropriate ICD codes. By itself, absence of . In a severe case, this results in pituitary hormone deficiencies, blindness, and mental retardation. ICD-10-CM/PCS MS-DRG v34.0 Definitions Manual: Skip to content: Appendix C: Principal diagnoses which convert CC/MCC to non-CC . Septo-optic dysplasia (SOD) is characterized by optic nerve hypoplasia, pituitary gland hypoplasia, and midline abnormalities of the brain.

Septo-optinen dysplasia (SOD) on harvinainen, synnynninen ja kliinisesti heterogeeninen oireyhtym, johon kuuluvat nkhermon vajaakehitys, hypopituitarismi eli aivoliskkeen vajaatoiminta sek puutteet keskiaivojen rakenteissa. Anencephaly O35.0XX1/Q00. . Congenital cerebral cysts. Create codetable from scratch Show conversion to ICD-9-CM NL - FR Contact .

ICD-10 Organisation OpenSAFELY Codelist ID opensafely/icd-10-chapter-xvii Version ID 7fed2e05. The 2022 edition of ICD-10-CM Q04.4 became effective on October 1, 2021. Septo-optic dysplasia of brain: Q04.5: Megalencephaly: Q04.6: Congenital cerebral cysts: Porencephaly Schizencephaly: Excludes1: acquired porencephalic cyst : . Septo-optic dysplasia: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: Other specified congenital malformations of brain: Q049: Congenital malformation of brain, unspecified: Q05: Strictly speaking, the Greek term translates as "without a brain" (or totally . Optic nerve hypoplasia (ONH) is a congenital disorder characterized by underdevelopment (hypoplasia) of the optic nerves. The clinical findings are visual impairment, hypopituitarism and developmental Septo-optic dysplasia of brain.

This page contains information about ICD-10 code: Q048.Diagnosis. Porencephaly; Schizencephaly (Q 048) Other specified congenital malformations of brain (Q 049) Congenital malformation of brain, unspecified (Q 05) Spina bifida (Q 06) Other congenital malformations of spinal cord (Q 060) Amyelia (Q 061) Hypoplasia and . . Normally, the forebrain is formed and the face begins to develop in the fifth and sixth weeks of human pregnancy.The condition also occurs in other species.

Septo-optic dysplasia of brain HTML | TXT | ICD-10 ⇄ ICD-9 CROSSWALK Q048 (Diagnosis) Other specified congenital malformations of brain . Hypoplasia and dysplasia of spinal cord: Q063: Other congenital cauda equina malformations: Q068: Dysplasia; Dysplasia ICD-10-CM Alphabetical Index.

Definition Septo-optic dysplasia (SOD) is a rare disorder characterized by abnormal development of the optic disk, pituitary deficiencies, and often agenesis (absence) of the septum pellucidum (the part of the brain that separates the anterior horns or the lateral ventricles of the brain).

The ICD-10 Code Q048 is assigned to Diagnosis "Other specified congenital malformations of brain". Septo-optic dysplasia. Overview.

Many times, de Morsier's Syndrome or septo-optic dysplasia (SOD) is associated with ONH, however, it is possible to have ONH without any additional issues like SOD. Septo-optic dysplasia of brain: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: Other specified congenital malformations of brain: Q049: BILLABLE Q04.4 Septo-optic dysplasia of brain ; BILLABLE Q04.5 Megalencephaly ; BILLABLE Q04.6 Congenital cerebral cysts ; . Initials ICD 10 Descriptor Q01.1 Nasofrontal encephalocele Q01.2 Occipital encephalocele Q02 Microcephaly Q03.0 Malformations of aqueduct of Sylvius Q03.1 Atresia of foramina of Magendie and Luschka Q04.2 Holoprosencephaly Q04.4 Septo-optic dysplasia of brain Q04.5 Megalencephaly Q05.0- Q05.3 and Q05.5- Q05.8 Spina bifida, Septo-optic dysplasia of brain: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: .

Septo-optic dysplasia of brain: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: Other specified congenital malformations of brain: Q050: Cervical spina bifida with hydrocephalus: Q051: Thoracic spina bifida with hydrocephalus: Septo-optic dysplasia is a heterogeneous condition with optic nerve hypoplasia, dysgenesis of the septum pellucidum, and pituitary hypofunction. . . ICD-10-CM Diagnosis Codes Q01-* Q01 Encephalocele.

It is found in the 2022 version of the ICD-10 Clinical Modification (CM) and can be used in all HIPAA-covered transactions from Oct 01, 2021 - Sep 30, 2022 .

Prognosis When the absence of the septum pellucidum is part of septo-optic dysplasia, the prognosis varies according to the presence and severity of associated symptoms. Case A has pituitary-optic dysplasia, and Case B has septo-optic dysplasia.

Septo-optic dysplasia O35.0XX1/Q04.4 Vein of Galen aneurysm O35.0XX1/Q28.2 CRANIAL Acrania O35.0XX1/Q00. Septo-optic dysplasia has been linked to young maternal age. dysplasia of remaining hematopoesis and/or myelodysplastic disease in its history C92.A- multilineage dysplasia C92.A-Marshall's ectodermal dysplasia (hidrotic) Q82.4 Neoplasia intraepithelial (histologically confirmed) cervix (uteri) (CIN) (histologically confirmed) N87.9 grade III (severe dysplasia) --see also Carcinoma, cervix uteri, in situ . Injury of optic tract and pathways . 2022 ICD-10-CM Diagnosis Code Q04.4 Septo-optic dysplasia of brain 2016 2017 2018 2019 2020 2021 2022 Billable/Specific Code POA Exempt Q04.4 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Applicable To. It has a near equal distribution among males and females, and it is typically diagnosed in newborns and infants.

Abnormalities of the white or grey matter, hydrocephalus, septo-optic dysplasia (Fig. Access to this feature is available in the following products: Find-A-Code Essentials HCC Plus Children were

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septo-optic Q04.4 skin L98.8 spinal cord Q06.1 spondyloepiphyseal Q77.7 thymic, with immunodeficiency D82.1 vagina N89.3 mild N89.0 moderate N89.1 severe NEC D07.2 vulva N90.3 mild N90.0 moderate N90.1 severe NEC D07.1 Hypoplasia and dysplasia of spinal cord: Q063: Other congenital cauda equina malformations: Q068: Optic nerve hypoplasia (ONH) is a congenital condition in which the optic nerve is underdeveloped (small). ICD-10 Diagnosis Codes .

Table D.2 Eye Malformations ICD-10-CM Diagnosis Codes Birth Defect ICD-10-CM 2. Septo-optic dysplasia (SOD) ( de Morsier syndrome) is a congenital malformation syndrome manifested by hypoplasia (underdevelopment) of the optic nerve, hypopituitarism, and absence of the septum pellucidum (a midline part of the brain ). ICD-10 Code for Septo-optic dysplasia of brain- Q04.4- Codify by AAPC Home Codes ICD-10 ICD-10-CM Codes Congenital malformations, deformations and chromosomal abnormalities Congenital malformations of the nervous system Other congenital malformations of brain (Q04) Septo-optic dysplasia of brain (Q04.4) Q04.3 Q04.4 Q04.5 OMIM 182230. . Q04.4 - Septo-optic dysplasia of brain; Q04.5 - Megalencephaly; Q04.6 - Congenital cerebral cysts; Q04.8 - Other specified congenital malformations of brain; . Septo-optic dysplasia (SOD) ( de Morsier syndrome) is a congenital malformation syndrome manifested by hypoplasia (underdevelopment) of the optic nerve, hypopituitarism, and absence of the septum pellucidum (a midline part of the brain ). ICD-10-CM, 10th ed., Centers for Medicare and Medicaid Services and the National Center for Health Statistics, 2018. Q04.4 Septo-optic dysplasia of brain ICD-10-CM Diagnosis Codes Q04.4 - Septo-optic dysplasia of brain The above description is abbreviated.

Q04.5. Case A. This 10-year-old girl was the product of a 42-week gestation, weighing 4.3 kg at birth. Q04.6.

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arrhythmogenic I42.8 septo-optic Q04.4 skin L98.8 spinal cord Q06.1 spondyloepiphyseal Q77.7 thymic, .

Brite: Human diseases [BR:br08402] Congenital malformations Congenital malformations of the nervous system H00544 Septo-optic dysplasia Human diseases in ICD-11 classification [BR:br08403] 20 . Septo-optic dysplasia is the name given to the condition where a child is diagnosed with two or more of the following problems: optic nerve hypoplasia, midline brain abnormalities and pituitary gland abnormalities. Q04.4 - Septo-optic dysplasia of brain Code Code Tree Map to The most common features are underdevelopment (hypoplasia) of the eye (optic) nerve, abnormal formation of structures along the midline of the brain such as the absence of the septum pellucidum and the corpus callosum, and a small pituitary (pituitary hypoplasia). Diseases-10 (ICD-10; W orld Health Organisation, 2006) standardised definitions. Currarino syndrome is an inherited congenital disorder where either the sacrum (the fused vertebrae forming the back of the pelvis) is not formed properly, or there is a mass in the presacral space in front of the sacrum, and there are malformations of the anus or rectum.It occurs in approximately 1 in 100,000 people. ICD-9-CM ICD-10-CM. Q01.0 Frontal encephalocele; Q01.1 Nasofrontal encephalocele; Q01.2 Occipital encephalocele; Q01.8 Encephalocele of other sites; Q01.9 Encephalocele, unspecified; ICD-10-CM Diagnosis Codes Q02-* Q02 Microcephaly; POA Indicators on CMS form 4010A are as follows: The ICD code Q044 is used to code Septo-optic dysplasia Optic nerve hypoplasia (ONH) is an important cause of congenital visual impairment in children and infants.

Septo-optic dysplasia is a disorder of early brain and eye development. Most people with ONH have abnormal eye movements (nystagmus) and vision can range from no light perception to good . While absence of the septum pellucidum is not associated with specific cognitive or developmental abnormalities, visual loss and . Septo-optic [icd-code.org] Other congenital malformations of brain Q04.0 Congenital malformations of corpus callosum Q04.2 Holoprosencephaly Q04.3 Other reduction deformities of brain Q04.4 Septo-optic [healthprovidersdata . . . ICD-10 Q04.4 ICD-9 743.57 OMIM 182230 DiseasesDB 32732 Septo-optic dysplasia(SOD) (de Morsier syndrome)[1][2]is a congenitalmalformationsyndromemanifested by hypoplasia (underdevelopment) of the optic nerve, hypopituitarism, and absence of the septum pellucidum(a midline part of the brain). Optic nerve hypoplasia, sensory integration dysfunction, septo-optic dysplasia, visual impairment. Septo-optic dysplasia of brain: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: . ICD-10-CM/PCS MS-DRG v39.0 Definitions Manual: Skip to content: .

Septo-optic dysplasia of brain ICD-10-CM Diagnosis Code S06.2X Diffuse traumatic brain injury ICD-10-PCS Procedure Code 3E0Q Cranial Cavity and Brain ICD-10-PCS Procedure Code 3E1Q Cranial Cavity and Brain ICD-10-PCS Procedure Code D020HZZ [convert to ICD-9-CM] Stereotactic Particulate Radiosurgery of Brain . The ICD-10-CM code Q04.4 might also be used to specify conditions or terms like congenital hypoplasia of cerebrum, hypoplasia of optic disc or septo-optic dysplasia sequence. There is no single cause of septo-optic dysplasia. The Icd-10 code range for Congenital malformations of the nervous system Q00-Q07 is medical classification list by the World Health Organization (WHO) Select. Septo-optic dysplasia is a developmental disorder resulting from a defect of normal embryological development. . septo-optic Q04.4 skin L98.8 spinal cord Q06.1 spondyloepiphyseal Q77.7 thymic, with immunodeficiency D82.1 vagina N89.3 mild N89.0 moderate N89.1 severe NEC D07.2 vulva N90.3 mild N90.0 moderate N90.1 severe NEC D07.1 Ectodermal dysplasia (anhidrotic) Q82.4 It is a rare condition affecting around 1 in every 10,000 births, with boys and girls affected equally. GARD 7627.

mesh; icd-10; umls data. This article discusses the observations and experiences of a multidisciplinary team at the Blind Childrens Center in Los Angeles, which works specifically with children from birth to 5 years of age who have been diagnosed with optic nerve hypoplasia and may have septo-optic displasia.

Septo-optic dysplasia of brain: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: Other specified congenital malformations of brain: Q049: ICD-10-CM code Q04 for Other congenital malformations of brain - Non-billable. Septo-optic dysplasia of brain: Q045: CC: 1055:4 codes: Megalencephaly: Q046: CC: 1055:4 codes: Congenital cerebral cysts: Q048: CC:

ICD-9-CM ICD-10-CM.

Septo-optic Dysplasia (SOD), also known as de Morsier Syndrome, is characterised by Optic Nerve Hypoplasia (ONH), pituitary hypoplasia and midbrain abnormalities such as absence of septum pellucidum and corpus collasum agenesis. In a severe case, this results in pituitary hormone deficiencies, blindness, and mental retardation. 7fed2e05 About; . Septo-optic dysplasia. Q04.6 - Congenital cerebral cysts. ICD-10-CM/PCS MS-DRG v34.0 Definitions Manual: Skip to content: Appendix C: Principal diagnoses which convert CC/MCC to non-CC . Anencephaly is the absence of a major portion of the brain, skull, and scalp that occurs during embryonic development. Absence of the SP alone is not a disorder but is instead a characteristic noted in children with septo-optic dysplasia or other developmental anomalies. It is a cephalic disorder that results from a neural tube defect that occurs when the rostral (head) end of the neural tube fails to close, usually between the 23rd and 26th day following conception. It is a unilateral or bilateral malformation of the optic nerve with a wide spectrum of severity. Septo-optic dysplasia (SOD), also known as de Morsier syndrome, . ICD-10-CM/PCS MS-DRG v39.0 Definitions Manual: Skip to content: MDC 01 Diseases and disorders of the nervous system: Other disorders of nervous system: . | ICD-10 from 2011 - 2016 Q04.4 is a billable ICD code used to specify a diagnosis of septo-optic dysplasia of brain. Septo-optic dysplasia is a rare congenital anomaly and has a reported prevalence of 6.3 per 100,000.

The optic nerves transmit impulses from the nerve-rich membranes lining the retina of the eye to the brain. ICD-10 Q04.4. Anterior sacral meningocele is the most common presacral mass in patients . Coding Notes for Q04 Info for medical coders on how to properly use this ICD-10 code. Fovea plana is the absence of a foveal pit in the central fovea, and despite . Anomalies of eye: 743.8; Syndromes of . Septo-optic dysplasia is a disorder of early brain development. . The code is exempt from present on admission (POA) reporting for inpatient admissions to general acute care hospitals. Strategies for educational interventions are explained. Q04.4 Septo-optic dysplasia of brain Septo-optic dysplasia sequence De Morsier syndrome 742.4 Q04.5 Megalencephaly Enlarged brain and/or head Macrocephaly Macroencephaly 742.4 Q04.6 Congenital cerebral cyst(s) Colloid cyst of third ventricle Congenital pseudoporencephaly Porencephaly Schizencephaly (m) Congenital choroid plexus cyst Q04.4 Septo-optic dysplasia of brain 742.3 Congenital hydrocephalus Q03.0 Malformations of aqueduct of Sylvius Q03.1 Atresia of foramina of Magendie and Luschka septo-optic Q04.4 skin L98.8 spinal cord Q06.1 spondyloepiphyseal Q77.7 thymic, with immunodeficiency D82.1 vagina N89.3 mild N89.0 moderate N89.1 severe NEC D07.2 vulva N90.3 mild N90.0 moderate N90.1 severe NEC D07.1 It has numerous clinical correlates, including neurologic and endocrine pathologies, making timely clinical diagnosis and further . Abnormal palmar creases; Accessory skin tags; Benign familial pemphigus [Hailey-Hailey] Congenital poikiloderma; Cutis laxa (hyperelastica) The portal uses cookies to provide service functions such as "Bookmark" and improve website usage.

Anterior sacral meningocele is the most common presacral mass in patients . Megalencephaly.

Septo-optic dysplasia of brain ICD-10-CM Diagnosis Code S06.2X Diffuse traumatic brain injury ICD-10-PCS Procedure Code 3E0Q Cranial Cavity and Brain ICD-10-PCS Procedure Code 3E1Q Cranial Cavity and Brain ICD-10-PCS Procedure Code D020HZZ [convert to ICD-9-CM] Stereotactic Particulate Radiosurgery of Brain Q04.8 - Other specified congenital malformations of brain. 1), and corpus callosum anomalies have been described.7 ONH can be unilateral or bilateral and can account for 15-25% of children with significant congenital visual loss.8 In addition, some investigators believe that foetal exposure to teratogenic agents . Septo-optic dysplasia of brain. [6] Holoprosencephaly (HPE) is a cephalic disorder in which the prosencephalon (the forebrain of the embryo) fails to develop into two hemispheres, typically occurring between the 18th and 28th day of gestation. POA Exempt Q04.4 is exempt from POA reporting ( Present On Admission). Septo-optic dysplasia of brain: Q045: Megalencephaly: Q046: Congenital cerebral cysts: Q048: Other specified congenital malformations of brain : PDX Collection 1056: E7871: Barth syndrome: