Neurologie

Illnesses according to ICD

Service ICD number Number of cases Info
Mixed specific developmental disorders F83 233
Cerebral palsy - Spastic quadriplegic cerebral palsy G80.0 43
Specific developmental disorders of speech and language - Developmental disorder of speech and language unspecified F80.9 27
Cerebral palsy - Spastic hemiplegic cerebral palsy G80.2 19
Specific developmental disorders of speech and language - Expressive language disorder F80.1 16
Cerebral palsy - Spastic diplegic cerebral palsy G80.1 15
Pervasive developmental disorders - Retts syndrome F84.2 12
Epilepsy G40.9 11
Down syndrome - Down syndrome unspecified Q90.9 11
Epilepsy G40.4 9
Cerebral palsy - Cerebral palsy unspecified G80.9 9
Hyperkinetic disorders - Attention-deficit hyperactivity disorder predominantly inattentive type F90.0 8
Other congenital malformations of brain - Other reduction deformities of brain Q04.3 8
Other specified congenital malformation syndromes affecting multiple systems Q87.1 8
Cerebral palsy - Athetoid cerebral palsy G80.3 7
Cerebral palsy - Other cerebral palsy G80.8 7
Hemiplegia G81.9 7
Other disorders of brain - Anoxic brain damage not elsewhere classified G93.1 7
Other chromosome abnormalities not elsewhere classified - Other specified chromosome abnormalities Q99.8 7
Pervasive developmental disorders - Autistic disorder F84.0 6
Unspecified disorder of psychological development F89 6
Epilepsy G40.8 6
Primary disorders of muscles G71.0 6
Intracranial injury S06.9 6
Specific developmental disorders of speech and language F80.8 5
Pervasive developmental disorders - Pervasive developmental disorder unspecified F84.9 5
Encephalitis myelitis and encephalomyelitis G04.8 5
Epilepsy G40.2 5
Other specified congenital malformation syndromes affecting multiple systems - Congenital malformation syndromes predominantly affecting facial appearance Q87.0 5
Down syndrome - Trisomy 21 nonmosaicism meiotic nondisjunction Q90.0 5
Monosomies and deletions from the autosomes not elsewhere classified - Deletion from autosomes unspecified Q93.9 5
Other chromosome abnormalities not elsewhere classified - Fragile X chromosome Q99.2 5
Encephalitis myelitis and encephalomyelitis G04.9 4
Hereditary ataxia - Early-onset cerebellar ataxia G11.1 4
Spinal muscular atrophy and related syndromes - Other inherited spinal muscular atrophy G12.1 4
Inflammatory polyneuropathy - Guillain-Barre syndrome G61.0 4
Cerebral palsy - Ataxic cerebral palsy G80.4 4
Hemiplegia G81.1 4
Lumbar spina bifida with hydrocephalus Q05.2 4
Other specified congenital malformation syndromes affecting multiple systems Q87.8 4
Monosomies and deletions from the autosomes not elsewhere classified Q93.5 4
Atypical virus infections of central nervous system - Subacute sclerosing panencephalitis A81.1 not specified
Malignant neoplasm of brain - Malignant neoplasm of occipital lobe C71.4 not specified
Malignant neoplasm of brain - Malignant neoplasm of brain stem C71.7 not specified
Malignant neoplasm of brain - Malignant neoplasm of brain unspecified C71.9 not specified
Lymphangioma any site D18.10 not specified
Benign neoplasm of brain and other parts of central nervous system - Benign neoplasm of brain infratentorial D33.1 not specified
Benign neoplasm of brain and other parts of central nervous system - Benign neoplasm of central nervous system unspecified D33.9 not specified
Neoplasm of uncertain or unknown behaviour of brain and central nervous system - Neoplasm of uncertain behavior of brain unspecified D43.2 not specified
Neoplasm of uncertain or unknown behaviour of endocrine glands - Neoplasm of uncertain behavior of craniopharyngeal duct D44.4 not specified
Hypoparathyroidism - Pseudohypoparathyroidism E20.1 not specified
Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism E71.1 not specified
Other disorders of carbohydrate metabolism E74.2 not specified
Other disorders of carbohydrate metabolism - Disorders of pyruvate metabolism and gluconeogenesis E74.4 not specified
Personality and behavioural disorders due to brain disease damage and dysfunction - Personality change due to known physiological condition F07.0 not specified
Personality and behavioural disorders due to brain disease damage and dysfunction F07.2 not specified
Reaction to severe stress and adjustment disorders F43.1 not specified
Mild mental retardation F70.0 not specified
Specific developmental disorders of speech and language - Phonological disorder F80.0 not specified
Mixed receptive-expressive language disorder F80.20 not specified
Mixed receptive-expressive language disorder F80.28 not specified
Specific developmental disorders of scholastic skills - Specific reading disorder F81.0 not specified
Specific developmental disorders of scholastic skills - Developmental disorder of scholastic skills unspecified F81.9 not specified
Specific developmental disorder of motor function F82.0 not specified
Specific developmental disorder of motor function F82.1 not specified
Specific developmental disorder of motor function F82.2 not specified
Specific developmental disorder of motor function F82.9 not specified
Pervasive developmental disorders F84.1 not specified
Pervasive developmental disorders - Aspergers syndrome F84.5 not specified
Hyperkinetic disorders - Attention-deficit hyperactivity disorder predominantly hyperactive type F90.1 not specified
Hyperkinetic disorders - Attention-deficit hyperactivity disorder unspecified type F90.9 not specified
Conduct disorders - Conduct disorder adolescent-onset type F91.2 not specified
Conduct disorders - Other conduct disorders F91.8 not specified
Emotional disorders with onset specific to childhood - Separation anxiety disorder of childhood F93.0 not specified
Enuresis not due to a substance or known physiological condition F98.02 not specified
Encephalitis myelitis and encephalomyelitis - Bacterial meningoencephalitis and meningomyelitis not elsewhere classified G04.2 not specified
Hereditary ataxia - Cerebellar ataxia with defective DNA repair G11.3 not specified
Hereditary ataxia - Hereditary spastic paraplegia G11.4 not specified
Hereditary ataxia - Hereditary ataxia unspecified G11.9 not specified
Spinal muscular atrophy and related syndromes - Infantile spinal muscular atrophy type I Werdnig-Hoffman G12.0 not specified
Spinal muscular atrophy and related syndromes - Spinal muscular atrophy unspecified G12.9 not specified
Other degenerative diseases of nervous system not elsewhere classified - Alpers disease G31.81 not specified
Other demyelinating diseases of central nervous system - Other specified demyelinating diseases of central nervous system G37.8 not specified
Epilepsy G40.09 not specified
Epilepsy G40.3 not specified
Migraine G43.1 not specified
Transient cerebral ischemic attack unspecified G45.99 not specified
Hereditary and idiopathic neuropathy - Hereditary motor and sensory neuropathy G60.0 not specified
Hereditary and idiopathic neuropathy - Hereditary and idiopathic neuropathy unspecified G60.9 not specified
Inflammatory polyneuropathy G61.8 not specified
Myasthenia gravis and other myoneural disorders - Congenital and developmental myasthenia G70.2 not specified
Primary disorders of muscles - Congenital myopathies G71.2 not specified
Primary disorders of muscles - Mitochondrial myopathy not elsewhere classified G71.3 not specified
Other myopathies G72.80 not specified
Hemiplegia G81.0 not specified
Paraplegia and tetraplegia G82.01 not specified
Paraplegia and tetraplegia G82.09 not specified
Paraplegia and tetraplegia G82.19 not specified
Paraplegia and tetraplegia G82.33 not specified
Paraplegia and tetraplegia G82.43 not specified
Paraplegia and tetraplegia G82.49 not specified
Paraplegia and tetraplegia G82.59 not specified
Other paralytic syndromes G83.1 not specified
Hydrocephalus - Hydrocephalus unspecified G91.9 not specified
Other disorders of brain - Postviral fatigue syndrome G93.3 not specified
Other disorders of brain G93.4 not specified
Other disorders of brain - Disorder of brain unspecified G93.9 not specified
Disorders of refraction and accommodation H52.2 not specified
Rheumatic chorea - Rheumatic chorea without heart involvement I02.9 not specified
Other pulmonary heart diseases - Pulmonary heart disease unspecified I27.9 not specified
Cardiomyopathy - Dilated cardiomyopathy I42.0 not specified
Cardiomyopathy - Obstructive hypertrophic cardiomyopathy I42.1 not specified
Intracerebral haemorrhage - Nontraumatic intracerebral hemorrhage in hemisphere unspecified I61.2 not specified
Intracerebral haemorrhage - Other nontraumatic intracerebral hemorrhage I61.8 not specified
Intracerebral haemorrhage - Nontraumatic intracerebral hemorrhage unspecified I61.9 not specified
Cerebral infarction I63.3 not specified
Cerebral infarction I63.8 not specified
Other cerebrovascular diseases - Moyamoya disease I67.5 not specified
Other cerebrovascular diseases - Cerebral arteritis not elsewhere classified I67.7 not specified
Other sac aneurysm or fissures of the layers of a blood vessel wall or a heart chamber - Aneurysm of carotid artery I72.0 not specified
Pneumonia due to Haemophilus influenzae J14 not specified
Adult respiratory distress syndrome J80.03 not specified
J80.06 not specified
Other diseases of stomach and duodenum - Disease of stomach and duodenum unspecified K31.9 not specified
Acute pancreatitis - Acute pancreatitis with uninfected necrosis unspecified K85.91 not specified
Dermatopolymyositis M33.0 not specified
Dermatopolymyositis M33.1 not specified
Other neuromuscular dysfunction of bladder N31.88 not specified
P77 not specified
Other disturbances of cerebral status of newborn - Neonatal cerebral leukomalacia P91.2 not specified
Other disturbances of cerebral status of newborn P91.6 not specified
Other congenital malformations of brain - Congenital malformations of corpus callosum Q04.0 not specified
Other congenital malformations of brain - Congenital cerebral cysts Q04.6 not specified
Other congenital malformations of brain - Other specified congenital malformations of brain Q04.8 not specified
Spina bifida unspecified Q05.9 not specified
Arteriovenous malformation of cerebral vessels Q28.29 not specified
Congenital malformations of oesophagus - Atresia of esophagus with tracheo-esophageal fistula Q39.1 not specified
Congenital deformities of hip Q65.0 not specified
Other congenital musculoskeletal deformities - Other specified congenital musculoskeletal deformities Q68.8 not specified
Other congenital malformations of skull and face bones - Mandibulofacial dysostosis Q75.4 not specified
Congenital malformations of spine and bony thorax Q76.4 not specified
Congenital malformations of the musculoskeletal system not elsewhere classified - Congenital diaphragmatic hernia Q79.0 not specified
Congenital malformations of the musculoskeletal system not elsewhere classified - Exomphalos Q79.2 not specified
Congenital ichthyosis - Ichthyosis vulgaris Q80.0 not specified
Other congenital malformations of skin - Incontinentia pigmenti Q82.3 not specified
Phakomatoses not elsewhere classified Q85.0 not specified
Phakomatoses not elsewhere classified - Tuberous sclerosis Q85.1 not specified
Phakomatoses not elsewhere classified - Other phakomatoses not elsewhere classified Q85.8 not specified
Congenital malformation syndromes due to known exogenous causes not elsewhere classified - Fetal alcohol syndrome dysmorphic Q86.0 not specified
Other specified congenital malformation syndromes affecting multiple systems - Congenital malformation syndromes involving early overgrowth Q87.3 not specified
Other congenital malformations not elsewhere classified - Other specified congenital malformations Q89.8 not specified
Other congenital malformations not elsewhere classified - Congenital malformation unspecified Q89.9 not specified
Other trisomies and partial trisomies of the autosomes not elsewhere classified Q92.6 not specified
Other trisomies and partial trisomies of the autosomes not elsewhere classified - Trisomy and partial trisomy of autosomes unspecified Q92.9 not specified
Monosomies and deletions from the autosomes not elsewhere classified Q93.8 not specified
Other sex chromosome abnormalities male phenotype not elsewhere classified - Klinefelter syndrome karyotype 47 XXY Q98.0 not specified
Other chromosome abnormalities not elsewhere classified - Chromosomal abnormality unspecified Q99.9 not specified
Dysphagia R13.9 not specified
Other lack of coordination - Ataxia unspecified R27.0 not specified
Other symptoms and signs involving general sensations and perceptions - Other symptoms and signs involving general sensations and perceptions R44.8 not specified
Pain not elsewhere classified R52.2 not specified
Lack of expected normal physiological development R62.8 not specified
Fracture of skull and facial bones S02.9 not specified
Intracranial injury S06.21 not specified
Intracranial injury S06.30 not specified
Intracranial injury S06.33 not specified
Intracranial injury S06.8 not specified
Dislocation sprain and strain of joint and ligaments of hip S73.02 not specified
Unspecified multiple injuries T07 not specified
Effects of other external causes T75.1 not specified
Personal history of other diseases and conditions Z87.6 not specified
Transplanted organ and tissue status - Liver transplant status Z94.4 not specified
Other postsurgical states Z98.8 not specified