| Category 1 | CONGENITAL MORPHOLOGICAL DISORDERS |
| | Agenesis of Corpus Callosum |
| Anorectal Malformation |
| Apert Syndrome |
| Arnold-Chiari Syndrome |
| Arthrogryposis |
| Bladder Exstrophy |
| Caudal agenesis |
| Caudal Regression Syndrome |
| Cerebral Neuronal Migration Disorders |
| Charge Syndrome |
| Cloacal Exstrophy |
| Congenital Epispadias |
| Congenital Hydrocephalus |
| Dandy-Walker malformation |
| Developmental Cord Disorder |
| Hirschsprung’s Disease |
| Holoprosencephaly |
| Imperforate Anus |
| Incomplete Corpus Callosum/Aicardi Syndrome |
| Lissencephaly |
| Megalencephaly |
| Microcephaly |
| Neural tube defect |
| Polymicrogyria |
| Pontocerebellar Hypoplasia |
| Posterior Urethral Valve Syndrome |
| Prune Belly Syndrome |
| Sacral Agenesis |
| Schizencephaly |
| Spinal Agenesis |
| Spinal Dysraphism |
| Spinal Hemangioma |
| Syringobulbia |
| Syringomyelia |
| Tethered spinal cord |
| Vater Syndrome/Vacterl Syndrome |
| Velocardiofacial Syndrome |
| Category 2 | CEREBRAL PALSY |
| Dystonic Cerebral Palsy |
| Hereditary Spastic Paralysis |
| Spastic Quadriplegia |
| Mixed cerebral palsy |
| Category 3 | SYNDROMES ASSOCIATED WITH INTELLECTUAL IMPAIRMENT |
| 2-Hydroxyglutaric Aciduria |
| Alpers Disease |
| Angelman Syndrome |
| Alpha Thalassaemia X-linked intellectual disability Syndrome |
| Bardet Biedl Syndrome |
| Beare-Stevenson Syndrome |
| Cyclin Dependent Kinase-Like 5 Gene Mutation |
| Chime Syndrome |
| Chromosome 1 Deletion |
| Chromosome 5q deletion (Cri Du Chat Syndrome) |
| Chromosome 13q Deletion Syndrome |
| Chromosome 15q Duplication Syndrome |
| Chromosome 18q Deletion Syndrome |
| Chromosome 1p36 Deletion Syndrome/Mono 1p36 |
| Chromosome 22 Ring |
| Chromosome 2q Deletion Syndrome |
| Chromosome 6 Ring Syndrome |
| Chromosome 8 Inversion or Duplication |
| Chromosome 9p Deletion Syndrome |
| Chromosome 9q Deletion Syndrome |
| Chromosome 11q (Jacobsen Syndrome) |
| Chromosome Xp Duplication |
| Cockayne Syndrome |
| Coffin-Lowry Syndrome |
| Cognitive Impairment |
| Cohen Syndrome |
| Congenital disorders of glycosylation |
| Congenital Neurological Infections |
| Cornelia de Lange Syndrome |
| Costello Syndrome |
| Cowden Disease |
| Developmental Delay |
| Developmental Delay associated with Autism, Autism Spectrum Disorder and Aspergers Syndrome |
| Dravet Syndrome |
| Fragile X Syndrome |
| Fumarase Deficiency |
| GLUT1-Deficiency Syndrome |
| Glutaric Aciduria Type 1 |
| Goldenhar’s Syndrome |
| Hunter Syndrome |
| Hurler-Scheie Syndrome |
| Hypomyelination disorders |
| Joubert Syndrome |
| Kabuki Syndrome |
| Langer-Gideon Syndrome |
| Lawrence Moon Biedel Syndrome |
| Lennox-Gastaut Syndrome |
| Lesch-Nyhan Syndrome |
| Lowe Syndrome |
| Mannosidosis |
| Maple Syrup Urine Disease |
| Meningitis |
| Menkes Syndrome |
| Mitochondrial Dieases |
| Molybdenum Cofactor Deficiency |
| Mowat-Wilson Syndrome |
| Mucolipidosis IV |
| Myotonic Dystrophy (Type 1) |
| Neonatal Hypoxic ischaemic encephalopathy |
| Neonatal Onset Multisystem Inflammatory Disease |
| Neuronal ceroid lipofuscinosis |
| Normal Pressure Hydrocephalus |
| OHDO Syndrome |
| Opitz Trigonocephaly Syndrome |
| Ohtahara Syndrome |
| Ouvrier Syndrome |
| Pallister-Killian Mosaic Syndrome |
| Peroxisome Biogenesis Disorder |
| Phelan McDermid Syndrome/22q 13 Deletion Syndrome |
| Phenylketonuria |
| Prader-Willi Syndrome |
| Pyruvate Dehydrogenase Deficiency/Leigh’s Disease |
| Rasmussen’s Disease |
| Rett Syndrome |
| Rubinstein-Taybi Syndrome |
| Sensory Integration Disorder/Dysfunction |
| Smith-Lemli-Opitz Syndrome |
| Smith-Magenis Syndrome |
| Sotos Syndrome |
| Sturge-Weber Syndrome |
| Subcortical Band Heterotopia |
| Translocation of Chromosome 2 |
| Translocation Trisomy 5/18 |
| Trichothiodystrophy |
| Triploidy |
| Trisomy 10 |
| Trisomy 13 (Patau syndrome) |
| Trisomy 18 (Edward Syndrome) |
| Trisomy 20p |
| Trisomy 21 (Down Syndrome) |
| Trisomy 47 |
| Trisomy 4p |
| Trisomy 9 |
| Tuberous Sclerosis |
| Turner Syndrome |
| Urea Cycle Defect |
| Valproate Embryopathy |
| West Syndrome |
| Williams Syndrome |
| Wolf-Hirschhorn Syndrome |
| X-Linked Adrenoleukodystrophy |
| Young-Simpson Syndrome |
| Category 4 | PARAPLEGIA and QUADRIPLEGIA |
| Paraparesis |
| Spinal Cord Compression |
| Spinal Cord Infarction |
| Spinal Cord Damage |
| Tetraplegia |
| Transverse Myelitis |
| Category 5 | ACQUIRED NEUROLOGICAL CONDITIONS |
| Acquired Brain Injury |
| Acute disseminated encephalomyelitis |
| Adhesive Arachnoiditis |
| Alcoholic Encephalopathy |
| Alzheimer’s Disease |
| Amyloidosis |
| Arachnoiditis |
| Ascending Polyneuropathy |
| Astrocytoma |
| Autonomic Neuropathy |
| Basal Ganglia Infarction |
| Benign Meningioma |
| Brown-Sequard Syndrome |
| Cauda Equina compression syndrome |
| Cerebral Abscess |
| Cerebral Aneurysm |
| Cerebral Anoxia |
| Cerebral Toxoplasmosis |
| Cerebral Tumour |
| Cerebrovascular Disease |
| Chronic Hypoxia |
| Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) |
| Cortical-Basal Ganglionic Degeneration |
| Dementia (any cause) |
| Developmental/Motor Dyspraxia |
| Diabetic Autonomic Neuropathy |
| Diabetic Neuropathic Bladder |
| Dorsal Pontine Band Syndrome |
| Encephalitis |
| Ependymoma |
| Epilepsy |
| Focal Cerebral Degeneration |
| Glioblastoma Multiforme |
| Glioblastoma of Spine |
| Hepatic Encephalopathy |
| Hydrocephalus (communicating or non-communicating) |
| Hypoxic Brain Injury |
| Inoperable Neurogenic Incontinence |
| Intracerebral Haemorrhage (Subarachnoid Haemorrhage, Subdural Haematoma) |
| Korsakoff’s Syndrome |
| Lambert-Eaton Myasthenic syndrome |
| Lewi Body Disease |
| Macroencephaly |
| Malignant Meningioma |
| Meningoencephalitis |
| Metastatic Carcinoma with Neurological Syndrome |
| Multiple Systems Atrophy |
| Myopathy |
| Nemaline Myopathy |
| Oligodendroglioma |
| Pachymeningitis |
| Periventricular Leukomalacia |
| Picks Disease |
| Pilocytic Astrocytoma |
| Poliomyelitis |
| Polymyoneuropathy |
| Posterior Leuco Encephalopathy |
| Primary Dystonia (case by case) |
| Primary or secondary CNS B-cell neoplasm |
| Progressive supranuclear palsy |
| Progressive Systemic Sclerosis |
| Sacral Neuroplexy |
| Sacral Plexopathy |
| Schizophrenia (Catatonic) |
| Schwannoma |
| Spinal Canal Disease |
| Spinal Chordoma |
| Spinal Ependymoma |
| Spinal Tumour |
| Stroke/Cerebrovascular Accident (CVA) |
| Category 6 | DEGENERATIVE NEUROLOGICAL DISEASES |
| Alexander Disease |
| Amyotrophic Lateral Sclerosis |
| Ataxia Telangiectasia |
| Canavan disease |
| Cauda Equina Syndrome |
| Cervical Myelopathy |
| Creutzfeldt-Jakob Disease (CJD) |
| Cytochrome C Oxidase Deficiency |
| Dejerine-Sottas Disease |
| Demyelinating Neuropathy |
| Demyelination of White Matter |
| Fahr’s Disease |
| Friedreich’s Ataxia |
| Guillain Barre Syndrome |
| Huntington Chorea |
| Huntington Disease |
| Hypoxic Ischaemic Encephalopathy |
| Idiopathic Axonal Neuropathy |
| Krabbe disease |
| Kugelberg-Welander Syndrome |
| Machado Joseph Disease |
| Metachromatic Leukodystrophy |
| Mitochondrial Myopathy with Encephalopathy |
| Morquio Syndrome |
| Motor Neurone Disease |
| Multiple Sclerosis |
| Muscular Dystrophy |
| Myotonic dystrophy |
| Myoneural Disorders |
| Neuroaxonal Dystrophy |
| Neurofibromatosis NF |
| Neurogenic Bowel |
| Neuromyelitis optica |
| Niemann-Pick Disease Type C |
| Pallister-Hall Syndrome |
| Parkinson Disease |
| Parkinsonism |
| PEHO Syndrome (Progressive encephalopathy with oedema, hypsarrhythmia and optic atrophy) |
| Pelizaeus Merzbacher Disease |
| Primary Lateral Sclerosis |
| Progressive Supranuclear Palsy/Steele Richardson Syndrome |
| Sanfilippo Syndrome |
| Sarcoidosis of the Brain |
| Shy-Drager Syndrome |
| Spinal Cord Syndrome |
| Spinal Muscular Atrophy Type 1 |
| Spinal Muscular Atrophy Type 2 |
| Spinocerebellar Degeneration |
| Stiff-Mans Syndrome |
| Striato-Nigral Degeneration |
| Subacute sclerosing pan-encephalitis |
| Thiamine deficiency |
| Vascular Myelopathy |
| Vertebral Canal Stenosis |
| Vertebral Degeneration |
| Wallerian Degeneration of White Matter |
| Wilson’s Disease |
| Category 7 | BLADDER OR BOWEL INNERVATION DISORDERS |
| Atonic Bladder/Hypotonic Bladder |
| Bladder Innervation Urgency |
| Cystocele (not suitable for surgery) |
| Dysfunctional Voiding |
| Dystonic Bladder |
| Ectopia Vesica |
| Linear Sebaceous Nevus Genetic |
| Myasthenia Gravis |
| Neurogenic Bladder |
| Neuronal Intestinal Dysplasia |
| Neuropathic Bladder |
| Post Bladder Surgery |
| Prostatectomy with nerve removal or damage |
| Pudendal Nerve Palsy |
| Radical Prostatectomy |
| Schmidli Autonomic Neuropathy |
| Slow Transit Constipation |
| Smooth Muscle Myopathy |
| Sphincter Deficiency (anal or bladder) |
| Spinal Stenosis |