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Disease	Synonyms	Description	Articles	Phenotypes
cataract 38	CATC5; CTRCT38; autosomal recessive congenital cat.. [+] CATC5; CTRCT38; autosomal recessive congenital cataract 5; [-]	A cataract that has_material_basis_in homozygous m..[+] A cataract that has_material_basis_in homozygous mutation in the AGK gene on chromosome 7q34. [-]
cataract 39 multiple types	CTRCT39; autosomal dominant cataract 39 multiple t.. [+] CTRCT39; autosomal dominant cataract 39 multiple types; [-]	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the CRYGB gene on chromosome 2q34. [-]
cataract 4 multiple types	CCA3; congenital cataract cerulean type 3; catarac.. [+] CCA3; congenital cataract cerulean type 3; cataract 4 multiple types with or without microcornea; CTRCT4; [-]	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the gamma-D-crystallin gene (CRYGD) on chromosome 2q33. [-]
cataract 40	cataract 40 X-linked; CTRCT40; cataract 40 with or.. [+] cataract 40 X-linked; CTRCT40; cataract 40 with or without microcornea; [-]	A cataract that has_material_basis_in mutation in ..[+] A cataract that has_material_basis_in mutation in the NHS gene on chromosome Xp22. [-]
cataract 41	congenital nuclear type cataract 41; CTRCT41;	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16. [-]
cataract 42	A cataract that has_material_basis_in heterozygous.. [+] A cataract that has_material_basis_in heterozygous mutation in the CRYBA2 gene on chromosome 2q35.; CTRCT42; [-]	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the CRYBA2 gene on chromosome 2q35. [-]
cataract 43	CTRCT43;	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the UNC45B gene on chromosome 17q12. [-]	1 articles
cataract 44	CTRCT44; total early-onset cataract;	A cataract that has_material_basis_in homozygous m..[+] A cataract that has_material_basis_in homozygous mutation in the LSS gene on chromosome 21q22. [-]
cataract 45	CTRCT45;	A cataract that has_material_basis_in homozygous m..[+] A cataract that has_material_basis_in homozygous mutation in the SIPA1L3 gene on chromosome 19q13. [-]	1 articles	7 matches
cataract 46 juvenile-onset	juvenilae cataract Hutterite type; CTRCT46;	A cataract that has_material_basis_in homozygous m..[+] A cataract that has_material_basis_in homozygous mutation in the LEMD2 gene on chromosome 6p21. [-]
cataract 47	CTRCT47;	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the SLC16A12 gene on chromosome 10q23, characterized by progressive juvenile cataract with microcornea. [-]
cataract 48	CTRCT48;	A cataract that has_material_basis_in homozygous m..[+] A cataract that has_material_basis_in homozygous mutation in the DNMBP gene on chromosome 10q24 and is characterized by infantile or early-childhood cataracts and visual impairment. [-]
cataract 5 multiple types	CTRCT5;	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the gene that encodes heat-shock transcription factor-4 (HSF4) on chromosome 16q22. [-]
cataract 6 multiple types	age related cortical cataract 2; ARCC2; CTPP1; CTR.. [+] age related cortical cataract 2; ARCC2; CTPP1; CTRCT6; posterior polar cataract 1; [-]	A cataract that has_material_basis_in heterozygous..[+] A cataract that has_material_basis_in heterozygous mutation in the EPHA2 gene on chromosome 1p36. [-]
cataract 7	CCA1; Cerulean type cataract 7; CTRCT7; congenital.. [+] CCA1; Cerulean type cataract 7; CTRCT7; congenital Cerulean type cataract 1; [-]	A cataract that has_material_basis_in variation in..[+] A cataract that has_material_basis_in variation in the region 17q24. [-]
cataract 8 multiple types	CCV; CTRCT8; cataract, congenital, Volkmann type;	A cataract that has_material_basis_in variation in..[+] A cataract that has_material_basis_in variation in the region 1pter-p36.13. [-]
cataract 9 multiple types	autosomal recessive congenital cataract 1; catarac.. [+] autosomal recessive congenital cataract 1; cataract 9 multiple types with or without microcornea; CTRCT9; CATC1; [-]	A cataract that has_material_basis_in autosomal re..[+] A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22. [-]
catecholaminergic polymorphic ventricular tachycardia		A heart conduction disease characterized by adrene..[+] A heart conduction disease characterized by adrenergically induced ventricular tachycardia manifesting as syncope and sudden death during exercise, stress or catecholamine infusion without the presence of structural cardiac abnormalities. [-]	4 articles
catecholaminergic polymorphic ventricular tachycardia 1	CVPT1; arrhythmogenic right ventricular dysplasia .. [+] CVPT1; arrhythmogenic right ventricular dysplasia 2; [-]	A catecholaminergic polymorphic ventricular tachyc..[+] A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the RYR2 gene on chromosome 1q43. [-]
catecholaminergic polymorphic ventricular tachycardia 2	CVPT2;	A catecholaminergic polymorphic ventricular tachyc..[+] A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the CASQ2 gene on chromosome 1p13 [-]
catecholaminergic polymorphic ventricular tachycardia 3	CVPT3;	A catecholaminergic polymorphic ventricular tachyc..[+] A catecholaminergic polymorphic ventricular tachycardia that is characterized by early onset mortality and has_material_basis_in variation in the chromosomal region 7p22-p14. [-]
catecholaminergic polymorphic ventricular tachycardia 4	CVPT4;	A catecholaminergic polymorphic ventricular tachyc..[+] A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal dominant inheritance and has_material_basis_in heterozygous mutation in the CALM1 gene on chromosome 14q32. [-]
catecholaminergic polymorphic ventricular tachycardia 5	CVPT5;	A catecholaminergic polymorphic ventricular tachyc..[+] A catecholaminergic polymorphic ventricular tachycardia that is characterized by autosomal recessive inheritance and has_material_basis_in homozygous or compound heterozygous mutation in the TRDN gene on chromosome 6q22. [-]
cauda equina intradural extramedullary astrocytoma	Intradural Extramedullary Astrocytic tumor of the .. [+] Intradural Extramedullary Astrocytic tumor of the Cauda Equina; [-]	n_a
cauda equina neoplasm	tumor of the Cauda Equina;	n_a
cauda equina neuroendocrine tumor	Cauda equina neuroendocrine tumour; Spinal neuroen.. [+] Cauda equina neuroendocrine tumour; Spinal neuroendocrine tumors; [-]	A cauda equina neoplasm that is a slow-growing, we..[+] A cauda equina neoplasm that is a slow-growing, well-differentiated neuroendocrine tumor arising from the cauda equina. [-]
caudal regression syndrome	caudal dysplasia sequence; caudal regression seque.. [+] caudal dysplasia sequence; caudal regression sequence; sacral agenesis; sacral defect with anterior meningocele; caudal dysgenesis syndrome; [-]	A physical disorder that is characterized by impai..[+] A physical disorder that is characterized by impairment of the development of the lower half of the body. [-]
causalgia	Complex regional pain syndrome, type II (disorder).. [+] Complex regional pain syndrome, type II (disorder); Complex regional pain syndrome, type II; [-]	n_a
cavernous hemangioma	Cavernoma; Cavernous haemangioma (disorder); Caver.. [+] Cavernoma; Cavernous haemangioma (disorder); Cavernous hemangioma (morphologic abnormality); Cavernous hemangioma; Cavernous haemangioma; [-]	n_a
cavernous hemangioma of colon	Colonic Cavernous hemangioma;	n_a
cavernous hemangioma of face		n_a
cavernous hemangioma of orbit	Cavernous Angioma of orbit;	n_a
cavernous sinus meningioma	meningioma of the Cavernous sinus;	n_a
cavernous sinus thrombosis	Thrombosis of cavernous venous sinus (disorder); T.. [+] Thrombosis of cavernous venous sinus (disorder); Thrombosis of cavernous venous sinus; [-]	n_a
cecal benign neoplasm	cecum neoplasm; neoplasm of caecum;	An intestinal benign neoplasm that is located_in t..[+] An intestinal benign neoplasm that is located_in the cecum. [-]
cecal disease	disorder of cecum (disorder); disorder of cecum;	An intestinal disease located_in the cecum.
cecum adenocarcinoma	adenocarcinoma of cecum; adenocarcinoma of cecum (.. [+] adenocarcinoma of cecum; adenocarcinoma of cecum (disorder); Cecal adenocarcinoma; [-]	A cecum carcinoma that derives_from epithelial cel..[+] A cecum carcinoma that derives_from epithelial cells of glandular origin. [-]
cecum adenoma	caecum adenoma;	A cecal benign neoplasm that has_material_basis_in..[+] A cecal benign neoplasm that has_material_basis_in epithelial tissue with glandular origin. [-]
cecum cancer	malignant neoplasm of caecum; malignant tumor of t.. [+] malignant neoplasm of caecum; malignant tumor of the cecum; [-]	A large intestine cancer that is located_in the ce..[+] A large intestine cancer that is located_in the cecum. [-]
cecum carcinoma	Caecum carcinoma; Cecal cancer; carcinoma of cecum.. [+] Caecum carcinoma; Cecal cancer; carcinoma of cecum; [-]	A cecum cancer that has_material_basis_in abnormal..[+] A cecum cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells. [-]
cecum lymphoma	Cecal Lymphoma;	n_a
cefaclor allergy	Ceclor allergy; cephaclor allergy;	A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger cefaclor. [-]
cefixime allergy		A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger cefixime. [-]
cefotaxime allergy		A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger cefotaxime. [-]
ceftazidime allergy	Fortaz allergy; Tazicef allergy;	A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger ceftazidime. [-]
ceftriaxone allergy	rocephin allergy;	A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger ceftriaxone. [-]
cefuroxime allergy	cephuroxime allergy; Zinacef allergy;	A cephalosporin allergy that has_allergic_trigger ..[+] A cephalosporin allergy that has_allergic_trigger cefuroxime. [-]
celery allergy		A vegetable allergy triggered by celery (Apium gra..[+] A vegetable allergy triggered by celery (Apium graveolens). [-]
celiac disease	celiac sprue; idiopathic steatorrhea; coeliac dise.. [+] celiac sprue; idiopathic steatorrhea; coeliac disease; [-]	An autoimmune disease of gastrointestinal tract th..[+] An autoimmune disease of gastrointestinal tract that is caused by a reaction located_in small intestine to gliadin, a prolamin (gluten protein) found in wheat, and similar proteins found in the crops of the tribe Triticeae. The disease is associated with HLA-DQ gene. It has_symptom abdominal pain, has_symptom constipation, has_symptom diarrhea, has_symptom nausea and vomiting, and has_symptom loss of appetite. [-]
cell type benign neoplasm		A benign neoplasm that is classified by the type o..[+] A benign neoplasm that is classified by the type of cell or tissue from which it is derived. [-]	7 articles	4 matches

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