| Disease Browser
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Parent Node:
 Brain Diseases (D001927) |
..Starting node
.. Colpocephaly (C535973)
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Child Nodes:
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Sister Nodes: |
..Akinetic Mutism (D000405)
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..Amblyopia (D000550)  2
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..Amnesia, Transient Global (D020236)
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..Auditory Diseases, Central (D001304) 19
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..Baraitser Brett Piesowicz syndrome (C537905)
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..Basal Ganglia Diseases (D001480) 102
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..Beta-Ureidopropionase Deficiency (C563210)
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..Brain Abscess (D001922) 1
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..Brain Damage, Chronic (D001925) 13
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..Brain Death (D001926)
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..Brain Diseases, Metabolic (D001928) 244
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..Brain Edema (D001929) 1
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..Brain Injuries (D001930) 11
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..Brain Neoplasms (D001932) 30
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..Cerebellar Diseases (D002526) 162
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..Cerebrovascular Disorders (D002561) 108
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..Colpocephaly (C535973)
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..Crome syndrome (C536216)
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..Dementia (D003704) 73
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..Dermatoleukodystrophy (C538220)
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..Diffuse Cerebral Sclerosis of Schilder (D002549) 3
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..Encephalitis (D004660) 32
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..Encephalomalacia (D004678) 2
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..Epilepsy (D004827) 196
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..Granulomas, congenital cerebral (C537294)
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..Hashimoto's encephalitis (C535841)
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..Headache Disorders (D020773) 26
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..Hydrocephalus (D006849) 52
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..Hypothalamic Diseases (D007027) 80
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..Hypoxia, Brain (D002534) 2
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..Intracranial Hypertension (D019586) 57
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..Intracranial Hypotension (D019585)
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..Keratosis follicularis dwarfism cerebral atrophy (C536158)
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..Kluver-Bucy Syndrome (D020232) 1
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..Leukoencephalopathies (D056784) 70
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..Macrogyria, pseudobulbar palsy and mental retardation (C537722)
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..MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY (OMIM:613668)
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..Neu Laxova syndrome (C536405)
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..Neuroaxonal Dystrophies (D019150) 13
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..Non-lissencephalic cortical dysplasia (C536243)
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..RAJAB SYNDROME (OMIM:613658)
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..Rambaud Galian syndrome (C535283)
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..Sener syndrome (C537579)
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..Sepsis-Associated Encephalopathy (D065166)
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..Spastic Pseudosclerosis (C563024)
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..Subdural Effusion (D013353)
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..Thalamic Diseases (D013786) 1
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..Thyrocerebral-retinal syndrome (C536908)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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