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Genetic Conditions…
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© 2006 Betterchem Corp.
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[Index] | [Continue]
- CADASIL
- Canavan disease
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Cancer
- Cancer Family Syndrome see hereditary nonpolyposis colorectal cancer
- Cancer of breast see breast cancer
- Cancer of the bladder see bladder cancer
- Carboxylase Deficiency, Multiple, Late-Onset see biotinidase deficiency
- Cardio-auditory-syncope syndrome see Jervell and Lange-Nielsen syndrome
- Cardioauditory syndrome of Jervell and Lange-Nielsen see Jervell and Lange-Nielsen syndrome
- Cardiomyopathy see Noonan syndrome
- Carpal Tunnel Syndrome see hereditary neuropathy with liability to pressure palsies
- Cat cry syndrome see cri-du-chat syndrome
- CATCH22 see 22q11.2 deletion syndrome
- CAVD see congenital bilateral absence of vas deferens
- Caylor cardiofacial syndrome see 22q11.2 deletion syndrome
- CBAVD see congenital bilateral absence of vas deferens
- CDLS see Cornelia de Lange syndrome
- CEP see congenital erythropoietic porphyria
- Ceramide trihexosidase deficiency see Fabry disease
- Cerebelloretinal Angiomatosis, Familial see von Hippel-Lindau syndrome
- Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy see CADASIL
- Cerebral autosomal dominant ateriopathy with subcortical infarcts and leukoencephalopathy see CADASIL
- cerebral sclerosis see tuberous sclerosis
- Cerebroatrophic Hyperammonemia see Rett syndrome
- Cerebroside Lipidosis Syndrome see Gaucher disease
- CF see cystic fibrosis
- CH see congenital hypothyroidism
- Charcot disease see amyotrophic lateral sclerosis
- Charcot-Marie-Tooth disease
- Chondrodystrophia fetalis see achondroplasia
- Chondrodystrophy syndrome see achondroplasia
- Chondrodystrophy with sensorineural deafness see otospondylomegaepiphyseal dysplasia
- Chondroectodermal Dysplasia see Ellis-van Creveld syndrome
- Chondrogenesis imperfecta see achondrogenesis, type 2
- Choreoathetosis self-mutilation hyperuricemia syndrome see Lesch-Nyhan syndrome
- Chromosomal imbalance syndrome, pair 13, trisomy see Patau syndrome
- Chromosomal imbalance syndrome, pair 18, trisomy see Edwards syndrome
- chromosome 13 trisomy syndrome see Patau syndrome
- Classic Galactosemia see galactosemia
- Classical Ehlers-Danlos syndrome see Ehlers-Danlos syndrome, classical type
- Classical Niemann-Pick Disease see Niemann-Pick disease
- Classical Phenylketonuria see phenylketonuria
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Cleft Lip and Palate
- Cloverleaf skull with thanatophoric dwarfism see thanatophoric dysplasia, type 2
- CLS see Coffin-Lowry syndrome
- CMT see Charcot-Marie-Tooth disease
- Cockayne syndrome
- Coffin-Lowry syndrome
- collagenopathy, types II and XI
- Colon cancer, familial see familial adenomatous polyposis
- Colon Cancer, Familial Nonpolyposis see hereditary nonpolyposis colorectal cancer
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Colorectal Cancer
- Complete HPRT deficiency see Lesch-Nyhan syndrome
- Complete hypoxanthine-guanine phosphoribosyltransferase deficiency see Lesch-Nyhan syndrome
- Complete trisomy 18 syndrome see Edwards syndrome
- compression neuropathy see hereditary neuropathy with liability to pressure palsies
- Congenital Adrenal Hyperplasia see 21-hydroxylase deficiency
- congenital bilateral absence of vas deferens
- congenital erythropoietic porphyria
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Congenital Heart Disease
- congenital hereditary hematuria see Alport syndrome
- congenital hypomyelination see Charcot-Marie-Tooth disease, type 1; Charcot-Marie-Tooth disease, type 4
- congenital hypothyroidism
- congenital methemoglobinemia see methemoglobinemia, beta-globin type
- Congenital osteosclerosis see achondroplasia
- Congenital sideroblastic anaemia see X-linked sideroblastic anemia
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Connective Tissue Disorders
- Conotruncal anomaly face syndrome (CTAF) see 22q11.2 deletion syndrome
- Cooley's Anemia see beta thalassemia
- Copper storage disease see Wilson disease
- Copper transport disease see Menkes syndrome
- Coproporphyria, Hereditary see hereditary coproporphyria
- Coproporphyrinogen oxidase deficiency see hereditary coproporphyria
- Cornelia de Lange syndrome
- Cowden syndrome
- CPO deficiency see hereditary coproporphyria
- CPRO deficiency see hereditary coproporphyria
- CPX deficiency see hereditary coproporphyria
- Craniofacial dysarthrosis see Crouzon syndrome
- Craniofacial Dysostosis see Crouzon syndrome
- Cretinism see congenital hypothyroidism
- Creutzfeldt-Jakob Disease see prion disease
- cri-du-chat syndrome
- Crouzon syndrome
- Crouzon syndrome with acanthosis nigricans see Crouzonodermoskeletal syndrome
- Crouzonodermoskeletal syndrome
- CS see Cockayne syndrome; Cowden syndrome
- Curschmann-Batten-Steinert syndrome see myotonic dystrophy
- cutis gyrata syndrome of Beare-Stevenson see Beare-Stevenson cutis gyrata syndrome
- cystic fibrosis
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