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Disease	Synonyms	Description
cerebellar ataxia		A hereditary ataxia that is characterized by ataxi..[+] A hereditary ataxia that is characterized by ataxia originating in the cerebellum. [-]
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome	CAMRQ; CAMRQ syndrome; cerebellar ataxia and menta.. [+] CAMRQ; CAMRQ syndrome; cerebellar ataxia and mental retardation with or without quadrupedal locomotion; cerebellar ataxia, mental retardation, and disequilibrium syndrome; cerebellar ataxia, mental retardation, and dysequilibrium syndrome; DES; disequilibrium syndrome; dysequilibrium syndrome; Uner Tan syndrome; UTS; [-]	A syndrome characterized by congenital onset of no..[+] A syndrome characterized by congenital onset of nonprogressive cerebellar ataxia, disturbed equilibrium, and mental retardation, associated with cerebellar hypoplasia. [-]
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 1	CAMRQ syndrome 1; CAMRQ1; cerebellar ataxia and me.. [+] CAMRQ syndrome 1; CAMRQ1; cerebellar ataxia and mental retardation with or without quadrupedal locomotion 1; cerebellar ataxia, mental retardation, and disequilibrium syndrome 1; cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1; cerebellar hypoplasia, VLDLR-associated; DES-VLDLR; dysequilibrium syndrome-VLDLR; VLDLR cerebellar hypoplasia; VLDLR-associated cerebellar hypoplasia; VLDLR-CH; [-]	A cerebellar ataxia, impaired intellectual develop..[+] A cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the VLDLR gene, which encodes the very low density lipoprotein receptor, on chromosome 9p24.2. [-]
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2	CAMRQ syndrome 2; CAMRQ2; cerebellar ataxia and me.. [+] CAMRQ syndrome 2; CAMRQ2; cerebellar ataxia and mental retardation with or without quadrupedal locomotion 2; cerebellar ataxia, mental retardation, and disequilibrium syndrome 2; cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2; [-]	A cerebellar ataxia, impaired intellectual develop..[+] A cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome that has_material_basis_in homozygous mutation in the WDR81 gene on chromosome 17p13.3. [-]
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 4	CAMRQ syndrome 4; CAMRQ4; cerebellar ataxia and me.. [+] CAMRQ syndrome 4; CAMRQ4; cerebellar ataxia and mental retardation with or without quadrupedal locomotion 4; cerebellar ataxia, mental retardation, and disequilibrium syndrome 4; cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4; [-]	A cerebellar ataxia, impaired intellectual develop..[+] A cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATP8A2 gene on chromosome 13q12.13. [-]
cerebellar ataxia type 41	SCA41;	An autosomal dominant cerebellar ataxia that has_m..[+] An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the TRPC3 gene on chromosome 4q27. [-]
cerebellar ataxia type 42	SCA42;	An autosomal dominant cerebellar ataxia characteri..[+] An autosomal dominant cerebellar ataxia characterized by gait instability, dysarthria, nystagmus, and saccadic pursuits with variable age of onset and severity and slow progression that has_material_basis_in heterozygous mutation of the CACNA1G gene on chromosome 17q21. [-]
cerebellar ataxia type 43	SCA43;	An autosomal dominant cerebellar ataxia characteri..[+] An autosomal dominant cerebellar ataxia characterized by adult-onset, slowly progressive, gait and limb ataxia, often associated with peripheral neuropathy typically affecting the motor system that has_material_basis_in heterozygous mutation in MME on chromosome 3q25.2. [-]
cerebellar ataxia type 47	SCA47;	An autosomal dominant cerebellar ataxia characteri..[+] An autosomal dominant cerebellar ataxia characterized by adult onset of slowly progressive cerebellar ataxia or in some cases earlier onset of ataxia accompanied by delayed motor development and short stature that has_material_basis_in heterozygous mutation in the PUM1 gene on chromosome 1p35.2. [-]
cerebellar ataxia type 48	SCA48;	An autosomal dominant cerebellar ataxia characteri..[+] An autosomal dominant cerebellar ataxia characterized by mid-adult onset of gait ataxia and/or cognitive-affective symptoms that has_material_basis_in heterozygous mutation in the STUB1 gene on chromosome 16p13.3. [-]
cerebellar ataxia type 9	SCA9;	An autosomal dominant cerebellar ataxia characteri..[+] An autosomal dominant cerebellar ataxia characterized by adult onset of ataxia and imbalance and demyelinating lesions on brain MRI. [-]
cerebellar atrophy, visual impairment, and psychomotor retardation	CAVIPMR;	A syndrome that is characterized by cerebellar atr..[+] A syndrome that is characterized by cerebellar atrophy, visual impairment and psychomotor retardation and that has_material_basis_in homozygous mutation in the EMC1 gene on chromosome 1p36. [-]
cerebellar disease		A brain disease that is characterized by damage to..[+] A brain disease that is characterized by damage to brain substance located_in cerebellum; has_symptom ataxia, has_symptom dysarthria, and has_symptom cerebellar cognitive affective syndrome. [-]
cerebellar hyplasia/atrophy, epilepsy, and global developmental delay		A syndrome with a cerebellar malformation as a maj..[+] A syndrome with a cerebellar malformation as a major feature characterized by cerebellar hypoplasia, bilateral retinal pigmentary changes, intellectual disability that can range from mild to moderate and pronounced language development delay. It presents with early developmental delay, central and peripheral non-progressive visual impairment or asymptomatic retinal changes, hypotonia, non-progressive ataxia and nystagmus. [-]
cerebellar hypoplasia		A cerebellar disease that is characterized by a ce..[+] A cerebellar disease that is characterized by a cerebellum that is smaller than usual or not completely developed. [-]
cerebellar liponeurocytoma	Cerebellar liponeurocytoma; Lipomatous Medulloblas.. [+] Cerebellar liponeurocytoma; Lipomatous Medulloblastoma; [-]	A cerebellum cancer that is characterized by consi..[+] A cerebellum cancer that is characterized by consistent neuronal, variable astrocytic and focal lipomatous differentiation. [-]
cerebellar medulloblastoma		A cerebellum cancer that begins in the lower part ..[+] A cerebellum cancer that begins in the lower part of the brain on the floor of the skull. [-]
cerebellar vermis medulloblastoma	Vermis Medulloblastoma;	n_a
cerebellofaciodental syndrome	cerebellar-facial-dental syndrome;	A syndrome that is characterized by delayed develo..[+] A syndrome that is characterized by delayed development, intellectual disability, abnormal facial and dental findings, and cerebellar hypoplasia and that has_material_basis_in homozygous or compound heterozygous mutation in the BRF1 gene on chromosome 14q32. [-]
cerebellopontine angle meningioma	Cerebellopontine angle meningioma (disorder); meni.. [+] Cerebellopontine angle meningioma (disorder); meningioma of the Cerebellar Pontine Angle; [-]	n_a
cerebellopontine angle primitive neuroectodermal tumor	Cerebellopontine Angle PNET;	n_a
cerebellopontine angle tumor	Cerebellopontine angle tumor (disorder); neoplasm .. [+] Cerebellopontine angle tumor (disorder); neoplasm of the Cerebellopontine Angle; cerebellopontine angle tumour; [-]	A brain stem cancer that is characterized by neopl..[+] A brain stem cancer that is characterized by neoplasms in the fossa located_in cerebellopontine angle. [-]
cerebellum cancer	cerebellar cancer; malignant tumor of Cerebellum;	n_a
cerebral amyloid angiopathy	dutch hereditary cerebral amyloid angiopathy; Here.. [+] dutch hereditary cerebral amyloid angiopathy; Hereditary cerebral haemorrhage with amyloidosis - Dutch type (disorder); Cerebral Hemorrhage, Hereditary, with Amyloidosis; Hereditary Cerebral Hemorrhage with Amyloidosis; [-]	An amyloidosis where amyloid protein progressively..[+] An amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes that usually result in spontaneous cerebral hemorrhage, ischemic lesions and progressive dementia. [-]
cerebral angioma	hemangioma of Cerebrum;	A brain angioma that is characterized by vascular ..[+] A brain angioma that is characterized by vascular abnormalities that develops from cranial and spinal blood vasculature, has_material_basis_in abnormally proliferating cells, derives_from endothelial cells in and about the vascular lumen. [-]
cerebral arterial disease		n_a
cerebral arteritis	Cerebral arteritis (disorder);	n_a
cerebral artery occlusion		A cerebrovascular disease that is characterized by..[+] A cerebrovascular disease that is characterized by blockage in one or more of the cerebral arteries. [-]
cerebral atherosclerosis	Cerebral atherosclerosis; Cerebral atherosclerosis.. [+] Cerebral atherosclerosis; Cerebral atherosclerosis (disorder); [-]	n_a
cerebral cavernous malformation	CCM; cavernous angiomatous malformations; cerebral.. [+] CCM; cavernous angiomatous malformations; cerebral capillary malformations; familial cavernous angioma; [-]	A cerebrovascular disease that is characterized by..[+] A cerebrovascular disease that is characterized by dilated blood-filled capillaries lacking structural support. [-]
cerebral cavernous malformation 1		A cerebral cavernous malformation that has_materia..[+] A cerebral cavernous malformation that has_material_basis_in heterozygous mutation in the KRIT1 gene on chromosome 7q21. [-]
cerebral cavernous malformation 2	CCM2;	A cerebral cavernous malformation that has_materia..[+] A cerebral cavernous malformation that has_material_basis_in mutation in the CCM2 gene on chromosome 7p13. [-]
cerebral cavernous malformation 3	CCM3;	A cerebral cavernous malformation that has_materia..[+] A cerebral cavernous malformation that has_material_basis_in mutation in the PDCD10 gene on chromosome 3q26.1. [-]
cerebral convexity meningioma	Cerebral Hemispheric Convexity meningioma;	n_a
cerebral creatine deficiency syndrome		An amino acid metabolic disorder that is character..[+] An amino acid metabolic disorder that is characterized by mental retardation, severe speech delay, behavioral abnormalities and seizures, has_material_basis_in mutation in the creatine transporter gene on chromosome Xq28. [-]
cerebral creatine deficiency syndrome 1	CEREBRAL CREATINE DEFICIENCY SYNDROME 1; SLC6A8 de.. [+] CEREBRAL CREATINE DEFICIENCY SYNDROME 1; SLC6A8 deficiency; creatine transporter deficiency; [-]	A cerebral creatine deficiency syndrome that is ch..[+] A cerebral creatine deficiency syndrome that is characterized by mental retardation, severe speech delay, behavioral abnormalities and seizures, has_material_basis_in mutation in the SLC6A8 gene on chromosome Xq28. [-]
cerebral degeneration	Brain degeneration;	A brain disease that is characterized by loss of s..[+] A brain disease that is characterized by loss of structure or function of neurons, including death of neurons and loss of brain tissue. [-]
cerebral falx meningioma	Falcine meningioma;	n_a
cerebral folate receptor alpha deficiency	Neurodegeneration due to cerebral folate transport.. [+] Neurodegeneration due to cerebral folate transport deficiency; [-]	A vitamin metabolic disorder that has_material_bas..[+] A vitamin metabolic disorder that has_material_basis_in mutations in the folate receptor 1 (FOLR1) gene coding for folate receptor alpha (FRalpha), is located_in the brain and is characterized by progressive movement disturbance, psychomotor decline, and epilepsy. [-]
cerebral hemisphere lipoma	Lipoma of the Cerebral Hemisphere;	n_a
cerebral infarction	Cerebral infarction; Cerebral infarction NOS; Cere.. [+] Cerebral infarction; Cerebral infarction NOS; Cerebral infarction NOS (disorder); Cerebral infarct; CVA - Cerebral infarction; [-]	A cerebrovascular disease that is characterized by..[+] A cerebrovascular disease that is characterized by an area of necrotic tissue in the brain resulting from a blockage or narrowing in the arteries supplying blood and oxygen to the brain. [-]
cerebral lipidosis		n_a
cerebral lymphoma	primary cerebral lymphoma (disorder); brain primar.. [+] primary cerebral lymphoma (disorder); brain primary lymphoma; primary Lymphoma of Cerebrum; primary cerebral lymphoma; [-]	A cerebrum cancer that affects the lymph cells and..[+] A cerebrum cancer that affects the lymph cells and derives_from the brain. [-]
cerebral malaria	Malarial encephalitis;	A malaria that involves neurologic damage resultin..[+] A malaria that involves neurologic damage resulting from blockage of the blood vessels, caused due to the infection of the red blood cells by Plasmodium species. [-]
cerebral meningioma	Cerebral meningioma (disorder); meningioma of Cere.. [+] Cerebral meningioma (disorder); meningioma of Cerebrum; [-]	n_a
cerebral neuroblastoma	neuroblastoma of brain (disorder); neuroblastoma o.. [+] neuroblastoma of brain (disorder); neuroblastoma of Cerebrum; neuroblastoma of brain; neuroblastoma of the cerebral hemisphere; [-]	A brain cancer that is characterized by small, rou..[+] A brain cancer that is characterized by small, round and blue cells with rosette patterns on histology, that has_material_basis_in abnormally proliferating cells and derives_from precursor cells called blast cells. [-]
cerebral palsy	infantile cerebral palsy;	A brain disease that is caused by damage to the mo..[+] A brain disease that is caused by damage to the motor control centers of the developing brain during pregnancy, during childbirth or after birth, which affects muscle movement and balance. [-]
cerebral primitive neuroectodermal tumor	PNET of Cerebrum;	n_a
cerebral ventricle cancer	cerebral ventricle neoplasm; Intraventricular tumo.. [+] cerebral ventricle neoplasm; Intraventricular tumor of brain; [-]	A cerebrum cancer that is located_in the cerebral ..[+] A cerebrum cancer that is located_in the cerebral ventricles. [-]
cerebritis		A brain disease that is characterized by inflammat..[+] A brain disease that is characterized by inflammation of the brain tissue occurring as a result of an underlying condition. [-]

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