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Disease	Synonyms	Description	Articles
corneal staphyloma		n_a
corneal ulcer		n_a
coronary aneurysm	Aneurysm of coronary vessels; Arteriovenous aneury.. [+] Aneurysm of coronary vessels; Arteriovenous aneurysm of coronary vessels; Aneurysmal lesion of coronary artery; [-]	n_a
coronary artery anomaly	Congenital anomaly of coronary artery (disorder); .. [+] Congenital anomaly of coronary artery (disorder); Coronary artery abnormality [Ambiguous]; Coronary artery anomaly NOS (disorder); Coronary artery abnormality (disorder); Congenital anomaly of coronary artery; Coronary artery abnormality; Coronary artery anomaly; Coronary artery anomaly, congenital; [-]	n_a
coronary artery disease	CHD (coronary heart disease); coronary arterioscle.. [+] CHD (coronary heart disease); coronary arteriosclerosis; CHD; coronary heart disease; Coronary disease; [-]	An artery disease that is characterized by plaque ..[+] An artery disease that is characterized by plaque building up along the inner walls of the arteries of the heart resulting in a narrowing of the arteries and a reduced blood supply to the cardiac muscles. [-]	3 articles
coronary artery vasospasm	Coronary artery spasm (disorder); Coronary Vasospa.. [+] Coronary artery spasm (disorder); Coronary Vasospasm; Coronary artery spasm; [-]	n_a
coronary restenosis		n_a
coronary stenosis	Coronary artery stenosis (disorder); Coronary arte.. [+] Coronary artery stenosis (disorder); Coronary artery stenosis; [-]	n_a
coronary thrombosis	Coronary artery thrombosis (disorder); Coronary ar.. [+] Coronary artery thrombosis (disorder); Coronary artery thrombosis; [-]	n_a
coronin-1A deficiency		A severe combined immunodeficiency that is an acti..[+] A severe combined immunodeficiency that is an actin regulator when mutated results in SCID through inhibition of thymic egress of mature thymocytes into peripheral lymphoid organs. [-]
corpus callosum agenesis-abnormal genitalia syndrome	ACC with abnormal genitalia; corpus callosum agene.. [+] ACC with abnormal genitalia; corpus callosum agenesis with abnormal genitalia; Proud syndrome; Proud-Levine-Carpenter syndrome; microcephaly-corpus callosum agenesis-abnormal genitalia syndrome; [-]	A syndrome characterized by agenesis of the corpus..[+] A syndrome characterized by agenesis of the corpus callosum, severe intellectual disability, seizures, and spasticity with males showing a severe phenotype and females showing a mild or non-affected phenotype that has_material_basis_in mutation in ARX on chromosome Xp21.3. [-]
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome	corpus callosum, agenesis of, with mental retardat.. [+] corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia; Graham-Cox syndrome; mental retardation, X-linked, syndromic 28; MRXS28; [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by agenesis of the corpus callosum, intellectual disability, ocular coloboma, micrognathia, sensorineural hearing loss, skeletal anomalies, and short stature that has_material_basis_in mutation in the IGBP1 gene on chromosome Xq13.1. [-]
corpus callosum lipoma	Lipoma of the Corpus Callosum;	n_a
corpus callosum oligodendroglioma		A brain oligodendroglioma located_in the corpus ca..[+] A brain oligodendroglioma located_in the corpus callosum. [-]
corpus luteum cyst		n_a
cortical blindness		n_a
cortical deafness		An agnosia that is a loss of the ability to percei..[+] An agnosia that is a loss of the ability to perceive any auditory information but whose hearing is intact. [-]
cortical dysplasia-focal epilepsy syndrome	CDFE syndrome; CDFES; Pitt-Hopkins-like syndrome-1.. [+] CDFE syndrome; CDFES; Pitt-Hopkins-like syndrome-1; PTHSL1; [-]	A brain disease that is characterized by cortical ..[+] A brain disease that is characterized by cortical dysplasia, focal epilepsy, macrocephaly, and diminished deep-tendon reflexes that has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the contactin associated protein like 2 (CNTNAP2) gene on chromosome 7q35-q36. [-]
cortical senile cataract	Cortical senile cataract;	A senile cataract that is characterized by opacifi..[+] A senile cataract that is characterized by opacification of the lens cortex, caused by dehydration of lens fibers, and is related to aging. [-]
corticobasal degeneration syndrome		A frontotemporal dementia that characterized by th..[+] A frontotemporal dementia that characterized by the loss of cognitive functions such as the ability to think, remember, or reason to the point that it interferes with a person's daily life and activities. [-]
corticosteroid-binding globulin deficiency	transcortin deficiency; CBG deficiency;	An adrenal gland disease characterized by decrease..[+] An adrenal gland disease characterized by decreased levels of serum corticosteroid-binding globulin and cortisol, and in some cases hypo- or hypertension, and muscle fatigue that has_material_basis_in heterozygous or homozygous mutation in the SERPINA6 gene on chromosome 14q32. [-]
corticosterone methyloxidase deficiency 1	aldosterone synthase deficiency;	An adrenal gland disease that is characterized by ..[+] An adrenal gland disease that is characterized by excessive amounts of sodium released in the urine, along with insufficient release of potassium in the urine, usually beginning in the first few weeks of life. [-]
cortisone reductase deficiency	CORTRD;	An endocrine system disease characterized by failu..[+] An endocrine system disease characterized by failure to regenerate the active glucocorticoid cortisol from cortisone resulting in adrenal hyperandrogenism. [-]
cortisone reductase deficiency 1	CORTRD1;	A cortisone reductase deficiency that has_material..[+] A cortisone reductase deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the H6PD gene on chromosome 1p36. [-]
cortisone reductase deficiency 2	CORTRD2;	A cortisone reductase deficiency that has_material..[+] A cortisone reductase deficiency that has_material_basis_in heterozygous mutation in the HSD11B1 gene on chromosome 1q32. [-]
cough variant asthma		A chronic asthma that is characterized by chronic ..[+] A chronic asthma that is characterized by chronic nonproductive cough without shortness of breath. [-]
cow milk allergy	Bos taurus milk allergy;	A milk allergy triggered by Bos taurus milk.
cowpox	yaba;	A viral infectious disease that results_in infecti..[+] A viral infectious disease that results_in infection in rodents, cows, and humans, located_in skin, has_material_basis_in Cowpox virus, which is transmitted_by contact with an infected animal. The infection results_in_formation_of vesicopustular lesions on the hands or face. [-]
cranial nerve III tumor	neoplasm of oculomotor nerve (disorder); Oculomoto.. [+] neoplasm of oculomotor nerve (disorder); Oculomotor nerve tumor; cranial nerve III tumour; Oculomotor nerve tumour; neoplasm of oculomotor nerve; [-]	n_a
cranial nerve disease	Cranial nerve disorder; disorder of cranial nerve;.. [+] Cranial nerve disorder; disorder of cranial nerve; [-]	A neuropathy that is located_in one of the twelve ..[+] A neuropathy that is located_in one of the twelve cranial nerves. [-]	2 articles
cranial nerve malignant neoplasm	malignant neoplasm of cranial nerves; malignant ne.. [+] malignant neoplasm of cranial nerves; malignant neoplasm of cranial nerves NOS (disorder); malignant tumor of cranial nerve (disorder); malignant tumor of the Cranial nerve; malignant tumor of cranial nerve; malignant neoplasm of cranial nerve; [-]	A central nervous system cancer that affects a cra..[+] A central nervous system cancer that affects a cranial nerve, develops from schwann cells located_in cranial nerves, has_material_basis_in abnormally proliferating cells. [-]
cranial nerve palsy	Cranial nerve Paralysis; Cranial nerve palsy;	A cranial nerve disease that is characterized by c..[+] A cranial nerve disease that is characterized by complete or partial weakness or paralysis of the areas served by the affected nerve. [-]
cranial pseudosarcomatous fasciitis		n_a
cranio-facial dystonia		A focal dystonia that is characterized as dystonia..[+] A focal dystonia that is characterized as dystonia that affects the muscles of the head, face, and neck. [-]	1 articles
craniodiaphyseal dysplasia		An osteosclerosis that results_in increased calciu..[+] An osteosclerosis that results_in increased calcium concentration located_in skull which decreases the size of cranium foramina and cervical spinal canal. [-]
cranioectodermal dysplasia	Levin syndrome; cranioectodermal dysplasia; Sensen.. [+] Levin syndrome; cranioectodermal dysplasia; Sensenbrenner syndrome; [-]	A syndrome that is characterized by characterized ..[+] A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies. [-]	1 articles
cranioectodermal dysplasia 4		A cranioectodermal dysplasia that has_material_bas..[+] A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR19 gene on chromosome 4p14. [-]
craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2		A craniofacial dysmorphism, skeletal anomalies, an..[+] A craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome that is characterized by flat face, low-set ears, and cleft lip and palate, as well as costovertebral anomalies including bifid and fused ribs, vertebral segmentation defects, and scoliosis. Intellectual delay can be severe, with absent speech and that has_material_basis_in homozygous mutation in the RAB5IF gene on chromosome 20q11. [-]
craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome	Cerebro-facio-thoracic dysplasia; Cerebrofaciothor.. [+] Cerebro-facio-thoracic dysplasia; Cerebrofaciothoracic dysplasia; Pascual-Castroviejo syndrome; TMCO1 defect syndrome; [-]	A syndrome that is characterized by abnormal devel..[+] A syndrome that is characterized by abnormal development of the brain and structures in the face and torso including facial dysmorphism, intellectual deficit costovertebral abnormalities, and delayed development of speech and movement (motor) skills. [-]	1 articles
craniofacial-deafness-hand syndrome	CDHS; Sommer-Young-Wee-Frye syndrome;	A syndrome characterized by a flat facial profile,..[+] A syndrome characterized by a flat facial profile, hypertelorism, a hypoplastic nose with slitlike nares, and sensorineural hearing loss that has_material_basis_in heterozygous mutation in the PAX3 gene on chromosome 2q36.1. [-]
craniofrontonasal syndrome	craniofrontonasal dysplasia; CFND; CFNS; craniofro.. [+] craniofrontonasal dysplasia; CFND; CFNS; craniofrontonasal dysostosis; [-]	A syndrome that has_material_basis_in mutation in ..[+] A syndrome that has_material_basis_in mutation in the EFNB1 gene on chromosome Xq13 and is characterized in hemizygous males by hypertelorism and with greater severity in females by frontonasal dysplasia, craniofacial asymmetry, craniosynostosis, bifid nasal tip, grooved nails, wiry hair, and abnormalities of the thoracic skeleton. [-]	2 articles
craniolenticulosutural dysplasia	Boyadjiev-Jabs Syndrome; cranio-lenticulo-sutural .. [+] Boyadjiev-Jabs Syndrome; cranio-lenticulo-sutural dysplasia, CLSD; [-]	A syndrome in neonates that is characterized by fa..[+] A syndrome in neonates that is characterized by facial dysmorphism, late-closing fontanels, cataract, and skeletal defects. It has_material_basis_in the mutation of the SEC23A gene on the 14th chromosome, with the underproduction in the collagen secreting pathway and distension of endoplasmic reticulum leading to bone defects. [-]
craniometaphyseal dysplasia		An osteosclerosis that has_material_basis_in mutat..[+] An osteosclerosis that has_material_basis_in mutations in the ANKH gene which results_in progressive thickening located_in skull and abnormally shaped ends of long bones in the limbs. [-]	1 articles
craniopharyngioma	craniopharyngioma (disorder); craniopharyngioma (m.. [+] craniopharyngioma (disorder); craniopharyngioma (morphologic abnormality); neoplasm of Rathke's Pouch; [-]	n_a
craniosynostosis	Premature closure of cranial sutures;	A synostosis that results_in premature fusion loca..[+] A synostosis that results_in premature fusion located_in skull. [-]	1 articles
craniosynostosis 7	CRS7;	A craniosynostosis characterized by skull deformit..[+] A craniosynostosis characterized by skull deformity and the inability of the skull's growth to keep up with the developing brain that has_material_basis_in a weakly penetrant heterozygous mutation in the SMAD6 gene on chromosome 15q22, typically with the risk allele of a common variant near the BMP2 gene on chromosome 20p12, resulting in potential intracranial pressure elevation. [-]
craniotubular dysplasia Ikegawa type	CTDI;	A craniodiaphyseal dysplasia characterized by chil..[+] A craniodiaphyseal dysplasia characterized by childhood-onset short stature in association with macrocephaly, dolichocephaly, or prominent forehead that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM53 gene on chromosome 1p34.1. [-]
crater-like holes of optic disc	Crater-like optic disc holes;	n_a
crescentic glomerulonephritis		n_a
cribriform carcinoma	ductal carcinoma, cribriform type; Cribriform carc.. [+] ductal carcinoma, cribriform type; Cribriform carcinoma; [-]	A breast carcinoma that is characterized by an irr..[+] A breast carcinoma that is characterized by an irregular cribriform growth pattern, nuclear grade I in at least 90% of cells, and absent myoepithelial cells. [-]

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