Nervous System Diseases | Page 3

1250 diseases found in 13 pages

C Diseases

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Cerebral folate deficiency Cerebral gigantism jaw cysts Cerebral palsy Cerebral palsy ataxic Cerebral palsy athetoid Cerebral palsy spastic hemiplegic Cerebral palsy spastic monoplegic Cerebral palsy spastic quadriplegic Cerebral sclerosis similar to Pelizaeus-Merzbacher disease Cerebro-facio-articular syndrome Cerebro-oculo-facio-skeletal syndrome Cerebrooculonasal syndrome Cerebrospinal fluid leak Cerebrotendinous xanthomatosis Ceroid lipofuscinosis neuronal 1 Cervical hypertrichosis peripheral neuropathy Chanarin-Dorfman syndrome Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2F Charcot-Marie-Tooth disease type 2G Charcot-Marie-Tooth disease type 2H Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2K Charcot-Marie-Tooth disease type 2N Charcot-Marie-Tooth disease type 2O Charcot-Marie-Tooth disease type 2P Charcot-Marie-Tooth disease type 2Q Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4H Chediak-Higashi syndrome Chiari malformation Chiari malformation type 1 Chiari malformation type 2 Chiari malformation type 4 Childhood apraxia of speech Childhood-onset nemaline myopathy Chorea-acanthocytosis Choroid plexus carcinoma Choroid plexus papilloma Christianson syndrome Chromosome 17p13.1 deletion syndrome Chromosome 17q11.2 deletion syndrome Chromosome 19q13.11 deletion syndrome Chromosome 1p36 deletion syndrome Chromosome 3p- syndrome Chronic hiccups Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids Chronic progressive external ophthalmoplegia Chudley Rozdilsky syndrome Cleft palate short stature vertebral anomalies Cluster headache COACH syndrome COASY Protein-Associated Neurodegeneration Coats disease Cobb syndrome Cockayne syndrome type I Cockayne syndrome type II Cockayne syndrome type III Coenzyme Q10 deficiency Coffin-Lowry syndrome Coffin-Siris syndrome COG1-CDG (CDG-IIg) COG4-CDG (CDG-IIj) COG5-CDG (CDG-IIi) COG7-CDG (CDG-IIe) COG8-CDG (CDG-IIh) Cohen syndrome Cold-induced sweating syndrome Complex regional pain syndrome Congenital central hypoventilation syndrome Congenital cytomegalovirus Congenital fiber type disproportion Congenital fibrosis of extraocular muscles Congenital generalized lipodystrophy type 4 Congenital insensitivity to pain Congenital insensitivity to pain with anhidrosis Congenital intrauterine infection-like syndrome Congenital laryngeal palsy Congenital mirror movement disorder Congenital muscular dystrophy due to LMNA mutation Congenital muscular dystrophy-dystroglycanopathy with or without intellectual disability (type B)

The RareGuru disease database is regularly updated using data generously provided by GARD, the United States Genetic and Rare Disease Information Center.

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