Disease Index
9,486 diseasescentral nervous system embryonal carcinoma
Human disease
central nervous system endodermal sinus tumor
Human disease
central nervous system ewing sarcoma/peripheral primitive neuroectodermal tumor
rare Ewing sarcoma/peripheral primitive neuroectodermal tumor that affects the central nervous system either as a primary dural neoplasm or by direct extension from adjacent soft tissues or bone
central nervous system germinoma
Human disease
central nervous system teratoma
Human disease
central nervous system vascular malformation
congenital, inherited, or acquired abnormalities involving arteries, veins or venous sinuses in the brain, spinal cord and meninges
MeSH: D020785
central nervous system vasculitis
Human disease
ICD: I67.7MeSH: D020293
central neurocytoma
Human disease
central polydactyly of fingers
human disease
central polydactyly of fingers, bilateral
human disease
central polydactyly of fingers, unilateral
human disease
central polydactyly of toes
human disease
central polydactyly of toes, bilateral
human disease
central polydactyly of toes, unilateral
human disease
central precocious puberty
MeSH: C562787
central retinal vein occlusion
Human disease
central serous retinopathy
eye disease that causes visual impairment, often temporary, usually in one eye; when the disorder is active, it is characterized by leakage of fluid under the retina that has a propensity to accumulate under the central macula
ICD: H35.7MeSH: D056833
centrifugal lipodystrophy
centripetalis recessive dystrophic epidermolysis bullosa
centronuclear myopathy
myopathy characterized by abnormally located nuclei in skeletal muscle cells
centronuclear myopathy X-linked
centronuclear myopathy that has material basis in X-linked inheritance of mutations in MTM1 on Xq28
cephalocele
human disease
cerebellar agenesis
human disease
cerebellar ataxia
cerebellar disease characterized by ataxia originating in the cerebellum.
ICD: G11.1MeSH: D002524
cerebellar ataxia type 43
human disease
cerebellar ataxia with peripheral neuropathy
human disease
cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome
medical condition
MeSH: C535351
cerebellar ataxia-ectodermal dysplasia syndrome
Cereballar ataxia - ectodermal dysplasia is a very rare disease, characterized by hypodontia and sparse hair in combination with cerebellar ataxia and normal intelligence. Imaging demonstrates a cerebellar atrophy.
MeSH: C535350
cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1
human disease
cerebellar hyplasia/atrophy, epilepsy, and global developmental delay
human disease