Service |
ICD number |
Number of cases |
Info |
Cerebral palsy - Spastic quadriplegic cerebral palsy |
G80.0 |
146
|
|
Cerebral palsy - Athetoid cerebral palsy |
G80.3 |
55
|
|
Other disorders of brain - Anoxic brain damage not elsewhere classified |
G93.1 |
51
|
|
Cerebral palsy - Cerebral palsy unspecified |
G80.9 |
36
|
|
Pervasive developmental disorders - Autistic disorder |
F84.0 |
24
|
|
Other disorders of brain |
G93.4 |
24
|
|
Epilepsy |
G40.4 |
22
|
|
Cerebral palsy - Spastic diplegic cerebral palsy |
G80.1 |
20
|
|
Paraplegia and tetraplegia |
G82.49 |
20
|
|
Cerebral palsy - Spastic hemiplegic cerebral palsy |
G80.2 |
19
|
|
Epilepsy |
G40.2 |
18
|
|
Lymphoid leukaemia - Acute lymphoblastic leukemia not having achieved remission |
C91.00 |
12
|
|
Encephalitis myelitis and encephalomyelitis |
G04.8 |
12
|
|
Epilepsy |
G40.9 |
12
|
|
Pervasive developmental disorders - Pervasive developmental disorder unspecified |
F84.9 |
11
|
|
Epilepsy |
G40.3 |
10
|
|
Hemiplegia |
G81.1 |
10
|
|
Cerebral palsy - Other cerebral palsy |
G80.8 |
9
|
|
Inflammatory polyneuropathy - Guillain-Barre syndrome |
G61.0 |
8
|
|
Monosomies and deletions from the autosomes not elsewhere classified |
Q93.5 |
8
|
|
Primary disorders of muscles - Congenital myopathies |
G71.2 |
7
|
|
Encephalitis myelitis and encephalomyelitis |
G04.9 |
6
|
|
Epilepsy |
G40.08 |
6
|
|
Spinal muscular atrophy and related syndromes - Infantile spinal muscular atrophy type I Werdnig-Hoffman |
G12.0 |
5
|
|
Other degenerative diseases of nervous system not elsewhere classified - Alpers disease |
G31.81 |
5
|
|
Epilepsy |
G40.8 |
5
|
|
Myasthenia gravis and other myoneural disorders - Congenital and developmental myasthenia |
G70.2 |
5
|
|
Other congenital malformations of brain - Other reduction deformities of brain |
Q04.3 |
5
|
|
Other congenital malformations of brain - Congenital malformation of brain unspecified |
Q04.9 |
5
|
|
Other specified congenital malformation syndromes affecting multiple systems |
Q87.1 |
5
|
|
Other specified congenital malformation syndromes affecting multiple systems |
Q87.8 |
5
|
|
Malignant neoplasm of brain - Malignant neoplasm of cerebellum |
C71.6 |
4
|
|
Specific developmental disorder of motor function |
F82.9 |
4
|
|
Pervasive developmental disorders - Retts syndrome |
F84.2 |
4
|
|
Unspecified disorder of psychological development |
F89 |
4
|
|
Epilepsy |
G40.1 |
4
|
|
Sleep disorders - Primary central sleep apnea |
G47.31 |
4
|
|
Hemiplegia |
G81.0 |
4
|
|
Intracerebral haemorrhage - Nontraumatic intracerebral hemorrhage unspecified |
I61.9 |
4
|
|
Intestinal malabsorption - Intestinal malabsorption unspecified |
K90.9 |
4
|
|
Other congenital malformations of brain - Congenital malformations of corpus callosum |
Q04.0 |
4
|
|
Tick-borne viral encephalitis - Central European tick-borne encephalitis |
A84.1 |
not specified
|
|
Other viral encephalitis not elsewhere classified - Other specified viral encephalitis |
A85.8 |
not specified
|
|
Herpesviral herpes simplex infections - Herpesviral encephalitis |
B00.4 |
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
|
|
Malignant neoplasm of spinal cord cranial nerves and other parts of central nervous system - Malignant neoplasm of spinal cord |
C72.0 |
not specified
|
|
Benign neoplasm of brain and other parts of central nervous system - Benign neoplasm of other specified parts of central nervous system |
D33.7 |
not specified
|
|
Immunodeficiency associated with other major defects - Di Georges syndrome |
D82.1 |
not specified
|
|
Thiamine deficiency - Wernickes encephalopathy |
E51.2 |
not specified
|
|
Disorders of aromatic amino-acid metabolism |
E70.2 |
not specified
|
|
Other disorders of amino-acid metabolism |
E72.1 |
not specified
|
|
Other disorders of amino-acid metabolism |
E72.2 |
not specified
|
|
Other disorders of amino-acid metabolism - Disorders of ornithine metabolism |
E72.4 |
not specified
|
|
Other disorders of carbohydrate metabolism |
E74.0 |
not specified
|
|
Disorders of sphingolipid metabolism and other lipid storage disorders |
E75.2 |
not specified
|
|
Disorders of glycosaminoglycan metabolism |
E76.2 |
not specified
|
|
Personality and behavioural disorders due to brain disease damage and dysfunction |
F07.1 |
not specified
|
|
Depressive episode - Major depressive disorder single episode severe with psychotic features |
F32.3 |
not specified
|
|
Mild mental retardation |
F70.1 |
not specified
|
|
Mild mental retardation |
F70.9 |
not specified
|
|
Other mental retardation |
F78.1 |
not specified
|
|
Unspecified mental retardation |
F79.8 |
not specified
|
|
Specific developmental disorder of motor function |
F82.0 |
not specified
|
|
Mixed specific developmental disorders |
F83 |
not specified
|
|
Pervasive developmental disorders |
F84.1 |
not specified
|
|
Pervasive developmental disorders - Other pervasive developmental disorders |
F84.8 |
not specified
|
|
Other disorders of psychological development |
F88 |
not specified
|
|
Hyperkinetic disorders - Attention-deficit hyperactivity disorder predominantly inattentive type |
F90.0 |
not specified
|
|
Hyperkinetic disorders - Attention-deficit hyperactivity disorder predominantly hyperactive type |
F90.1 |
not specified
|
|
Conduct disorders - Oppositional defiant disorder |
F91.3 |
not specified
|
|
Conduct disorders - Conduct disorder unspecified |
F91.9 |
not specified
|
|
Stereotyped movement disorders |
F98.40 |
not specified
|
|
Other specified behavioral and emotional disorders with onset usually occurring in childhood and adolescence |
F98.88 |
not specified
|
|
Bacterial meningitis not elsewhere classified - Streptococcal meningitis |
G00.2 |
not specified
|
|
Encephalitis myelitis and encephalomyelitis |
G04.0 |
not specified
|
|
Hereditary ataxia - Cerebellar ataxia with defective DNA repair |
G11.3 |
not specified
|
|
Hereditary ataxia - Hereditary spastic paraplegia |
G11.4 |
not specified
|
|
Spinal muscular atrophy and related syndromes - Other inherited spinal muscular atrophy |
G12.1 |
not specified
|
|
Spinal muscular atrophy and related syndromes - Spinal muscular atrophy unspecified |
G12.9 |
not specified
|
|
Dystonia - Genetic torsion dystonia |
G24.1 |
not specified
|
|
Other extrapyramidal and movement disorders |
G25.88 |
not specified
|
|
Other degenerative diseases of nervous system not elsewhere classified |
G31.88 |
not specified
|
|
Other degenerative diseases of nervous system not elsewhere classified - Degenerative disease of nervous system unspecified |
G31.9 |
not specified
|
|
Other demyelinating diseases of central nervous system - Acute transverse myelitis in demyelinating disease of central nervous system |
G37.3 |
not specified
|
|
Other demyelinating diseases of central nervous system - Other specified demyelinating diseases of central nervous system |
G37.8 |
not specified
|
|
Epilepsy |
G40.01 |
not specified
|
|
Epilepsy |
G40.5 |
not specified
|
|
Epilepsy |
G40.6 |
not specified
|
|
Status epilepticus |
G41.9 |
not specified
|
|
Sleep disorders - Other sleep apnea |
G47.39 |
not specified
|
|
Sleep disorders - Other sleep disorders |
G47.8 |
not specified
|
|
Other polyneuropathies |
G62.80 |
not specified
|
|
Myasthenia gravis and other myoneural disorders |
G70.8 |
not specified
|
|
Myasthenia gravis and other myoneural disorders - Myoneural disorder unspecified |
G70.9 |
not specified
|
|
Primary disorders of muscles |
G71.0 |
not specified
|
|
Primary disorders of muscles - Primary disorder of muscle unspecified |
G71.9 |
not specified
|
|
Other myopathies |
G72.80 |
not specified
|
|
Cerebral palsy - Ataxic cerebral palsy |
G80.4 |
not specified
|
|
Hemiplegia |
G81.9 |
not specified
|
|
Paraplegia and tetraplegia |
G82.03 |
not specified
|
|
Paraplegia and tetraplegia |
G82.13 |
not specified
|
|
Paraplegia and tetraplegia - Paraplegia complete |
G82.21 |
not specified
|
|
Paraplegia and tetraplegia |
G82.32 |
not specified
|
|
Paraplegia and tetraplegia |
G82.42 |
not specified
|
|
Paraplegia and tetraplegia |
G82.43 |
not specified
|
|
Paraplegia and tetraplegia - Quadriplegia C5-C7 complete |
G82.53 |
not specified
|
|
Other paralytic syndromes - Paralytic syndrome unspecified |
G83.9 |
not specified
|
|
Hydrocephalus - Hydrocephalus unspecified |
G91.9 |
not specified
|
|
Other disorders of brain - Disorder of brain unspecified |
G93.9 |
not specified
|
|
Other cardiac arrhythmias - Other specified cardiac arrhythmias |
I49.8 |
not specified
|
|
Intracerebral haemorrhage - Other nontraumatic intracerebral hemorrhage |
I61.8 |
not specified
|
|
Respiratory failure not elsewhere classified - Chronic respiratory failure with hypoxia |
J96.11 |
not specified
|
|
Respiratory failure not elsewhere classified |
J96.19 |
not specified
|
|
Respiratory failure not elsewhere classified |
J96.99 |
not specified
|
|
Other acquired deformities of limbs |
M21.50 |
not specified
|
|
Other joint disorders not elsewhere classified - Pain in unspecified joint |
M25.50 |
not specified
|
|
Scoliosis |
M41.29 |
not specified
|
|
Other deforming dorsopathies - Spondylolysis occipito-atlanto-axial region |
M43.01 |
not specified
|
|
Juvenile osteochondrosis of hip and pelvis |
M91.1 |
not specified
|
|
Other transitory neonatal electrolyte and metabolic disturbances - Late metabolic acidosis of newborn |
P74.0 |
not specified
|
|
Congenital hydrocephalus - Atresia of foramina of Magendie and Luschka |
Q03.1 |
not specified
|
|
Other congenital malformations of brain - Other specified congenital malformations of brain |
Q04.8 |
not specified
|
|
Lumbar spina bifida with hydrocephalus |
Q05.2 |
not specified
|
|
Spina bifida unspecified |
Q05.9 |
not specified
|
|
Other congenital malformations of nervous system |
Q07.0 |
not specified
|
|
Congenital malformations of larynx - Laryngeal hypoplasia |
Q31.2 |
not specified
|
|
Other congenital malformations of respiratory system - Other specified congenital malformations of respiratory system |
Q34.8 |
not specified
|
|
Congenital malformations of oesophagus - Atresia of esophagus without fistula |
Q39.0 |
not specified
|
|
Other congenital malformations of intestine - Persistent cloaca |
Q43.7 |
not specified
|
|
Congenital deformities of hip - Congenital dislocation of hip bilateral |
Q65.1 |
not specified
|
|
Congenital deformities of feet - Other congenital valgus deformities of feet |
Q66.6 |
not specified
|
|
Congenital deformities of feet |
Q66.8 |
not specified
|
|
Other congenital malformations of limbs - Arthrogryposis multiplex congenita |
Q74.3 |
not specified
|
|
Osteochondrodysplasia with defects of growth of tubular bones and spine - Chondrodysplasia punctata |
Q77.3 |
not specified
|
|
Other osteochondrodysplasias - Osteogenesis imperfecta |
Q78.0 |
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
|
|
Other specified congenital malformation syndromes affecting multiple systems - Congenital malformation syndromes predominantly affecting facial appearance |
Q87.0 |
not specified
|
|
Other specified congenital malformation syndromes affecting multiple systems - Other congenital malformation syndromes with other skeletal changes |
Q87.5 |
not specified
|
|
Down syndrome - Trisomy 21 nonmosaicism meiotic nondisjunction |
Q90.0 |
not specified
|
|
Down syndrome - Trisomy 21 translocation |
Q90.2 |
not specified
|
|
Down syndrome - Down syndrome unspecified |
Q90.9 |
not specified
|
|
Edwards syndrome and Patau syndrome - Trisomy 18 unspecified |
Q91.3 |
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 - Other specified trisomies and partial trisomies of autosomes |
Q92.8 |
not specified
|
|
Monosomies and deletions from the autosomes not elsewhere classified - Deletion of short arm of chromosome 4 |
Q93.3 |
not specified
|
|
Monosomies and deletions from the autosomes not elsewhere classified |
Q93.8 |
not specified
|
|
Monosomies and deletions from the autosomes not elsewhere classified - Deletion from autosomes unspecified |
Q93.9 |
not specified
|
|
Other chromosome abnormalities not elsewhere classified - Other specified chromosome abnormalities |
Q99.8 |
not specified
|
|
Other chromosome abnormalities not elsewhere classified - Chromosomal abnormality unspecified |
Q99.9 |
not specified
|
|
Dysphagia - Aphagia |
R13.0 |
not specified
|
|
Other lack of coordination - Ataxia unspecified |
R27.0 |
not specified
|
|
Other symptoms and signs involving the nervous and musculoskeletal systems |
R29.8 |
not specified
|
|
Other symptoms and signs involving cognitive functions and awareness |
R41.8 |
not specified
|
|
Lack of expected normal physiological development - Delayed milestone in childhood |
R62.0 |
not specified
|
|
Intracranial injury |
S06.20 |
not specified
|
|
Intracranial injury |
S06.21 |
not specified
|
|
Intracranial injury |
S06.28 |
not specified
|
|
Intracranial injury |
S06.31 |
not specified
|
|
Intracranial injury |
S06.5 |
not specified
|
|
Fracture of femur |
S72.00 |
not specified
|
|
Complications of other internal prosthetic devices implants and grafts |
T85.0 |
not specified
|
|