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Nume Hydrocephalus
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Atresia of foramina of Magendie and Luschka; Congenital hydrocephalus, unspecified; Hydrocephalus, unspecified; Malformations of aqueduct of Sylvius; Other congenital hydrocephalus
Clasificare anatomică Malacards Boli neuronale; Boli osoase
Boli din aceeaşi familie Hydrocephalus Autosomal Recessive; Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius; Hydrocephalus, Autosomal Dominant; Hydrocephalus, Nonsyndromic, Autosomal Recessive 1; Hydrocephalus, Nonsyndromic, Autosomal Recessive 2

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Boli A-Z Abducens Palsy Acalvaria Achondroplasia Acoustic Neuroma Acquired Immunodeficiency Syndrome Acrocallosal Syndrome Acromesomelic Dysplasia Adenocarcinoma Adenoma Adrenoleukodystrophy Adult Medulloblastoma Aging Agnosia Aicardi Syndrome Aids Dementia Complex Akinetic Mutism Aland Island Eye Disease Albinism Alcohol Abuse Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Echinococcosis Alzheimer Disease 2 Amenorrhea Amyloidosis, Finnish Type Anaplastic Ependymoma Anaplastic Ganglioglioma Anaplastic Oligodendroglioma Andersen Cardiodysrhythmic Periodic Paralysis Androgen Insensitivity Syndrome, Mild Anencephaly Aneurysm Aneurysmal Bone Cysts Angiomatosis Aniridia 1 Ankyloblepharon Filiforme Adnatum and Cleft Palate Anorexia Nervosa 1 Antiphospholipid Syndrome Aphasia Apnea, Obstructive Sleep Apraxia Arachnoid Cysts Arachnoiditis Arterial Tortuosity Syndrome Arteriovenous Fistula Arteriovenous Malformation Arthritis Arthrochalasia Ehlers-Danlos Syndrome Aseptic Meningitis Aspergillosis Asphyxiating Thoracic Dystrophy Astroblastoma Astrocytoma Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Atlantoaxial Subluxation Atrioventricular Septal Defect Atypical Follicular Adenoma Atypical Teratoid Rhabdoid Tumor Auditory Agnosia Ayme-Gripp Syndrome Bacterial Meningitis Baller-Gerold Syndrome Baraitser-Winter Syndrome 1 Barrett Esophagus Basaloid Squamous Cell Carcinoma Basilar Artery Occlusion B-Cell Lymphomas Beare-Stevenson Cutis Gyrata Syndrome Beemer Ertbruggen Syndrome Benign Ependymoma Beta-Adrenergic Stimulation, Response to Binswanger's Disease Blake Pouch Cyst Bleeding Disorder, Platelet-Type, 11 Blepharospasm Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Bobble-Head Doll Syndrome Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Brain Cancer Brain Edema Brain Glioma Brain Injury Brainstem Auditory Evoked Responses Brain Stem Glioma Branchial Arch Defects Brittle Bone Disorder Bronchiectasis Bronchopneumonia Burns Calvarial Hyperostosis Capillary Hemangioma Carcinoid Syndrome Cardiac Tamponade Carpal Tunnel Syndrome Cataract Cataract 5, Multiple Types Cat Eye Syndrome Cauda Equina Syndrome Cellular Ependymoma Central Cord Syndrome Central Nervous System Disease Central Nervous System Organ Benign Neoplasm Central Nervous System Primitive Neuroectodermal Neoplasm Central Nervous System Teratoma Central Neurocytoma Central Precocious Puberty Cerebellar Agenesis Cerebellar Astrocytoma Cerebellar Hypoplasia Cerebellar Liponeurocytoma Cerebellar Medulloblastoma Cerebellopontine Angle Meningioma Cerebellum Cancer Cerebral Amyloid Angiopathy, Cst3-Related Cerebral Aneurysms Cerebral Atrophy Cerebral Degeneration Cerebral Neuroblastoma Cerebral Ventricle Cancer Cerebritis Cerebrovascular Disease Cerebrum Cancer Cervicitis Chiari Malformation Chiari Malformation Type I Chiari Malformation Type Ii Choanal Atresia, Posterior Cholelithiasis Cholesteatoma Chorea, Childhood-Onset, with Psychomotor Retardation Choreatic Disease Chorioretinitis Choroiditis Choroid Plexus Cancer Choroid Plexus Cyst Chromosomal Triplication Chromosome 15q Deletion Chromosome 1q Deletion Chromosome 6q Deletion Chromosome 8q Duplication Chronic Meningitis Chudley-Mccullough Syndrome Ciliary Dyskinesia, Primary, 1 Ciliopathy Cinca Syndrome Clear Cell Ependymoma Cleft Lip Cleft Lip/palate Coccidioidomycosis Coffin-Lowry Syndrome Cole-Carpenter Syndrome Colitis Communicating Hydrocephalus Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cone-Rod Dystrophy 2 Congenital Communicating Hydrocephalus Congenital Cytomegalovirus Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi Congenital Non-Communicating Hydrocephalus Congenital Toxoplasmosis Congenital Varicella Syndrome Congenital Zika Syndrome Conjunctivitis Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Cortical Blindness Corticobasal Degeneration Cranial Nerve Palsy Craniopharyngioma Craniosynostosis Craniosynostosis with Fibular Aplasia Cri-Du-Chat Syndrome Crouzon Syndrome Crouzon Syndrome with Acanthosis Nigricans Cryoglobulinemia Cryptococcal Meningitis Cutis Laxa, Autosomal Recessive, Type Iiia Cutis Marmorata Telangiectatica Congenita Cysticercosis Cystic Teratoma Cystinosis Cytomegalovirus Infection Dandy-Walker Complex Dandy-Walker Syndrome Delusional Disorder Dementia Dermoid Cyst Desmoplastic Infantile Ganglioglioma Dextrocardia Diabetes Insipidus Diabetes Mellitus Diarrhea Diastematomyelia Duane Retraction Syndrome 1 Duodenal Atresia Duodenitis Dwarfism Dysembryoplastic Neuroepithelial Tumor Dystonia 9 Echinococcosis Eclampsia Ectodermal Dysplasia Empty Sella Syndrome Encephalitis Encephalocele Encephalomyopathy Encephalopathy Endocardial Fibroelastosis Endotheliitis Enophthalmos Eosinophilic Meningitis Ependymoblastoma Ependymoma Epidermoid Cysts Epilepsy Essential Tremor Exophthalmos Extraventricular Neurocytoma Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Familial Idiopathic Basal Ganglia Calcification Fanconi Anemia, Complementation Group E Faye-Petersen-Ward-Carey Syndrome Finger Agnosia Focal Dermal Hypoplasia Foix Chavany Marie Syndrome Frontal Convexity Meningioma Frontonasal Dysplasia 1 Frontotemporal Dementia Fungal Meningitis Gait Apraxia Galactosemia Galactosialidosis Game Friedman Paradice Syndrome Gangliocytoma Ganglioglioma Ganglioneuroma Gastrointestinal Stromal Tumor Gaucher Disease, Type I Gemistocytic Astrocytoma Giant Cell Glioblastoma Giant Cell Tumor Glioblastoma Glioblastoma Multiforme Gliofibroma Glioma Gliomatosis Cerebri Gliosarcoma Glomus Tumor Glutaric Acidemia I Granulomatous Angiitis Granulosa Cell Tumor of the Ovary Griscelli Syndrome Growth Hormone Deficiency Guillain-Barre Syndrome Hajdu-Cheney Syndrome Headache Headache Associated with Sexual Activity Head Injury Helix Syndrome Hellp Syndrome Hemangioblastoma Hemangioma Hemifacial Spasm Hemihyperplasia-Multiple Lipomatosis Syndrome Hemiplegia Hemolytic Anemia Hemophagocytic Lymphohistiocytosis Hemophilia Hepatic Adenomas, Familial Hepatitis Hepatitis C Herpes Simplex Herpes Zoster Herpes Zoster Ophthalmicus Heterotaxy, Visceral, 2, Autosomal Hip Subluxation Histiocytosis Histoplasmosis Holoprosencephaly Homocystinuria Huntington Disease Hydranencephaly Hydrocele Hydrocephalus Autosomal Recessive Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius Hydrocephalus, Endocardial Fibroelastosis, and Cataracts Hydrocephalus, Nonsyndromic, Autosomal Recessive 1 Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hydrocephalus, Normal-Pressure Hydrocephalus with Stenosis of the Aqueduct of Sylvius Hydromyelia Hydrops Fetalis Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperglycemia Hyperostosis Hypertelorism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertrichosis Hypertropia Hypervitaminosis a Hypoglossia-Hypodactylia Hypoglycemic Coma Hypopituitarism Hypothalamic Hamartomas Hypotonia Immunoglobulin E Concentration, Serum Infertility Influenza Insulin-Like Growth Factor I Intellectual Deficit Buenos-Aires Type Internuclear Ophthalmoplegia Intestinal Pseudo-Obstruction Intracranial Aneurysm Intracranial Cysts Intracranial Hypertension Intracranial Hypotension Ischemia Isolated Duane Retraction Syndrome Jackson-Weiss Syndrome Japanese Encephalitis Juvenile Pilocytic Astrocytoma Kleeblattschaedel Klippel-Feil Syndrome Kozlowski Brown Hardwick Syndrome Langerhans Cell Histiocytosis Larsen Syndrome Laryngitis Lateral Sinus Thrombosis Learning Disability Legius Syndrome Leiomyosarcoma Leukodystrophy Leukoencephalopathy, Hereditary Diffuse, with Spheroids Ligneous Conjunctivitis Lipid Pneumonia Lipomatosis Lissencephaly Listeria Meningitis Lobar Holoprosencephaly Locked-in Syndrome Lupus Erythematosus Lutheran Suppressor, X-Linked Lymphocytic Choriomeningitis Lymphoma Lymphosarcoma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Macs Syndrome Major Affective Disorder 8 Major Affective Disorder 9 Malaria Male Infertility Malignant Glioma Malignant Hypertension Malignant Peripheral Nerve Sheath Tumor Malignant Sertoli Cell Tumor Mannosidosis Masa Syndrome Mastoiditis Mature Teratoma Medulloblastoma Medulloepithelioma Medullomyoblastoma Megalencephaly Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 Megalocornea Melanoma Melanosis, Neurocutaneous Melanotic Neuroectodermal Tumor Meningeal Melanocytoma Meningeal Melanomatosis Meningioma, Familial Meningitis Meningocele Meningococcal Meningitis Meningoencephalitis Meningoencephalocele Metachromatic Leukodystrophy Microcephaly Middle Cerebral Artery Infarction Milia, Multiple Eruptive Mitochondrial Complex Iv Deficiency Miyoshi Muscular Dystrophy 1 Mongolian Spot Monosomy 9q22.3 Mucolipidosis Iv Mucopolysaccharidoses Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis Type Vi Mucopolysaccharidosis, Type Vii Muenke Syndrome Multiple Sclerosis Multiple Sulfatase Deficiency Multiple System Atrophy 1 Mumps Muscular Dystrophy Mutism Myelocystocele Myelomeningocele Myoclonus Myopathy Myotonic Dystrophy Neonatal Meningitis Neonatal Stroke Nephrocalcinosis Neural Tube Defects Neural Tube Defects, Folate-Sensitive Neurenteric Cyst Neurilemmoma of the Fifth Cranial Nerve Neuroblastoma Neurodegeneration with Brain Iron Accumulation 2a Neurofibroma Neurofibromatosis, Type Iv, of Riccardi Neuroleptic Malignant Syndrome Neuroma Neuronal Ceroid Lipofuscinosis Neuronitis Neurosarcoidosis Neurosyphilis Obsessive-Compulsive Disorder Obstructive Hydrocephalus Occipital Encephalocele Oligodendroglioma Opitz Gbbb Syndrome, Type Ii Opsismodysplasia Optic Nerve Glioma Optic Nerve Hypoplasia, Bilateral Optic Nerve Neoplasm Optic Papillitis Organ System Benign Neoplasm Osteochondrodysplasia Osteogenesis Imperfecta, Type Ii Osteoglophonic Dysplasia Osteopetrosis Otitis Media Oto-Palatal-Digital Syndrome Pachygyria Papillary Ependymoma Papilledema Papilloma Papilloma of Choroid Plexus Paraganglioma Parainfluenza Virus Type 3 Parametritis Paraplegia Parkinson Disease 15, Autosomal Recessive Early-Onset Penicillin Allergy Peritonitis Periventricular Nodular Heterotopia Persistent Vegetative State Peters-Plus Syndrome Pfeiffer Syndrome Phacomatosis Pigmentovascularis Pick Disease of Brain Pilocytic Astrocytoma Pineal Gland Cancer Pineocytoma Pituitary Adenoma Pituitary Hormone Deficiency, Combined, 2 Pituitary Tumors Plagiocephaly Plasminogen Deficiency, Type I Plasmodium Vivax Malaria Pleomorphic Xanthoastrocytoma Pneumococcal Meningitis Pneumonia Polydactyly Polymicrogyria Polyneuropathy Porencephaly Posterior Cortical Atrophy Precocious Puberty Pre-Eclampsia Premature Chromatid Separation Trait Primary Ciliary Dyskinesia Prion Disease Prosopagnosia Protein C Deficiency Proteus Syndrome Pseudo-Meigs Syndrome Pulmonary Edema Pycnodysostosis Radioulnar Synostosis Reactive Arthritis Regional Odontodysplasia Retinitis Rheumatoid Arthritis Rhombencephalosynapsis Ring Chromosome 6 Rothmund-Thomson Syndrome Sacrococcygeal Teratoma Sagittal Sinus Thrombosis Salt and Pepper Developmental Regression Syndrome Sarcoma Schizophrenia Sclerosing Cholangitis, Neonatal Scoliosis Scrapie Seizure Disorder Seizures, Benign Familial Neonatal, 1 Sella Turcica Neoplasm Semilobar Holoprosencephaly Senile Plaque Formation Short Bowel Syndrome Siderosis Sinusitis Sirenomelia Situs Inversus Skull Base Meningioma Sleep Apnea Small Cell Carcinoma Small Cell Neuroendocrine Carcinoma Sparganosis Spastic Diplegia Spasticity Spastic Paraparesis Speech Disorder Spina Bifida Aperta Spinal Cord Astrocytoma Spinal Cord Ependymoma Spinal Cord Infarction Spinal Cord Injury Spinal Cord Melanoma Spinal Stenosis Split-Hand/foot Malformation 1 Spondyloocular Syndrome Spontaneous Intracranial Hypotension Streptococcal Meningitis Strongyloidiasis Subcortical Arteriosclerotic Encephalopathy Subependymal Giant Cell Astrocytoma Subependymal Glioma Subependymoma Sulfhemoglobinemia Superficial Siderosis Suppression of Tumorigenicity 12 Supratentorial Cancer Sveinsson Chorioretinal Atrophy Syndrome of Inappropriate Antidiuretic Hormone Synostosis Syringobulbia Syringohydromyelia Syringomyelia Systemic Lupus Erythematosus Tanycytic Ependymoma Teeth Present at Birth Teratoma Tetanus Tetraamelia Syndrome, Autosomal Recessive Tetralogy of Fallot Thanatophoric Dysplasia, Type Ii Three M Syndrome 1 Thrombocytopenia Thrombosis Thumb Deformity Toxocariasis Toxoplasmoză Transient Global Amnesia Transposition of the Great Arteries Traumatic Brain Injury Treacher Collins Syndrome 1 Tremor Tremor, Hereditary Essential, and Idiopathic Normal Pressure Hydrocephalus Trigeminal Neuralgia Trisomy 22 Tuberculous Meningitis Tuberculum Sellae Meningioma Tuberous Sclerosis Ulcerative Colitis Urinary Bladder Small Cell Neuroendocrine Carcinoma Urinary System Disease Vaccinia Vacterl Association Vacterl Association with Hydrocephalus Vacterl Association with Hydrocephaly, X-Linked Vacterl with Hydrocephalus Vascular Dementia Vascular Disease Vasculitis Vein of Galen Aneurysm Vertebral Artery Occlusion Vesicoureteral Reflux 1 Vitreoretinopathy, Neovascular Inflammatory Walker-Warburg Syndrome West Syndrome X-Linked Complicated Spastic Paraplegia Type 1 Yemenite Deaf-Blind Hypopigmentation Syndrome