Conditions Search
Conditions starting from Ca to Ce
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'Ca to Ce' returned 302 records
- CACH Syndrome
- CADASIL
- Cafe-Au-Lait Macules with Pulmonary
- Caffey Disease
- CAHMR Syndrome
- Calcification of joints and arteries
- Calcifying Epithelial Odontogenic Tumor
- Calciphylaxis
- Calcium pyrophosphate deposition disease (CPDD)
- Calcium pyrophosphate dihydrate crystal deposition disease (CPPD)
- Calloso-Genital Dysplasia
- Calvarial Hyperostosis
- Camera Marugo Cohen Syndrome
- Campomelia Cumming Type
- Campomelic Dysplasia
- Camptobrachydactyly
- Camptocormism
- Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome
- Camptodactyly Joint Contractures and Facial Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly Syndrome Guadalajara Type 3
- Camptodactyly Taurinuria
- Camptodactyly Vertebral Fusion
- Camptodactyly, Fibrous Tissue Hyperplasia, and Skeletal Dysplasia
- Camptodactyly, Tall Stature, and Hearing Loss Syndrome
- Camptodactyly-Ichthyosis Syndrome
- Camptomelic dysplasia
- Camptomelic Syndrome Long Limb Type
- Camurati Engelmann Disease
- Camurati Engelmann disease type II
- Camurati Engelmann Disease, Type 2
- Camurati-Engelmann Disease
- Canavan Disease
- Cancer
- Cancer predisposition
- Cancer, Breast
- Cancer, Childhood
- Cancer, Colorectal
- Cancer, Head and Neck
- Cancer, Hereditary
- Cancer, Lung
- Cancer, Non-Polyposis Colorectal
- Cancer, Ovarian
- Cancer, Rectal
- Cancer, Salivary Gland
- Candida Glabrata
- Candidemia
- Candidiasis of the skin
- Candidiasis, familial, 2
- Candidiasis, familial, 4
- Candidiasis, familial, 5
- Candidiasis, familial, 6
- Candidiasis, familial, 7
- Canker sore
- CANOMAD Syndrome
- Cap disease
- Cap myopathy
- Capillary Hemangioblastoma
- Capillary malformation-arteriovenous malformation
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Carbamyl Phosphate Synthetase Deficiency
- Carbohydrate Deficient Glycoprotein Syndrome
- Carbohydrate-deficient glycoprotein syndrome type I
- Carbohydrate-deficient glycoprotein syndrome type II
- Carcinoid Syndrome
- Carcinoid tumor
- Carcinoid Tumor Childhood
- Carcinoid tumors, intestinal
- Cardiac arrhythmia, Ankyrin-B-related
- Cardiac asthma
- Cardiac Diverticulum
- Cardiac Hydatid Cysts with Intracavitary Expansion
- Cardiac Rupture
- Cardiac syndrome X
- Cardiac Valvular Dysplasia, X-Linked
- Cardio-neurogenic syncope
- Cardioauditory Syndrome of Sanchez Cascos
- Cardiocranial Syndrome
- Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency
- Cardiofaciocutaneous Syndrome
- Cardiogenic shock
- Cardiomegaly
- Cardiomyopathy
- Cardiomyopathy and Deafness due to tRNA Lysine Gene Mutation
- Cardiomyopathy Cataract Hip Spine Disease
- Cardiomyopathy Dilated with Conduction Defect Type 1
- Cardiomyopathy Dilated with Conduction Defect Type 2
- Cardiomyopathy Dilated with Woolly Hair and Keratoderma
- Cardiomyopathy due to Anthracyclines
- Cardiomyopathy Hypogonadism Collagenoma Syndrome
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Cardiomyopathy Spherocytosis
- Cardiomyopathy, dilated, 1gg
- Cardiomyopathy, dilated, 1hh
- Cardiomyopathy, dilated, 1t
- Cardiomyopathy, dilated, 1u
- Cardiomyopathy, dilated, 1v
- Cardiomyopathy, Dilated, 3A
- Cardioskeletal Syndrome Kuwaiti Type
- Cardiospasm
- Cardiovascular disease
- Carnevale Hernandez Castillo Syndrome
- Carnevale Syndrome
- Carney Complex
- Carney complex variant
- Carney complex, type 1
- Carnitine Almitoyltransferase I Deficiency, Muscle
- Carnitine Deficiency
- Carnitine Palmitoyl Transferase 1 Deficiency
- Carnitine Palmitoyl Transferase 2 Deficiency
- Carnitine Palmitoyltransferase Deficiency Type 1
- Carnitine Palmitoyltransferase Deficiency Type 2
- Carnitine palmitoyltransferase II deficiency, lethal neonatal
- Carnitine uptake defect
- Carnitine-Acylcarnitine Translocase Deficiency
- Carnosinemia
- Caroli Disease
- Carotenemia
- Carotid artery disease
- Carotid body tumor
- Carotid intimal medial thickness 1
- Carpal Deformity Migrognathia Microstomia
- Carpal tunnel syndrome
- Carpenter Hunter Type
- Carpenter Syndrome
- Carpo Tarsal Osteolysis Recessive
- Carpotarsal Osteochondromatosis
- Cartilage-Hair Hypoplasia
- Caspase-8 Deficiency
- Cassavism
- Castleman's Disease
- Cat Eye Syndrome
- Cat Scratch Disease
- Cat-Eye Syndrome
- Catamenial Pneumothorax
- Cataplexy
- Cataract and Cardiomyopathy
- Cataract and Congenital Ichthyosis
- Cataract Anterior Polar Dominant
- Cataract Ataxia Deafness
- Cataract Congenital Autosomal Dominant
- Cataract Congenital Dominant Non Nuclear
- Cataract Congenital Volkmann Type
- Cataract Hutterite Type
- Cataract Hypertrichosis Mental Retardation
- Cataract Mental Retardation Hypogonadism
- Cataract Microcornea Syndrome
- Cataract Microphthalmia Septal Defect
- Cataract, age-related cortical, 2
- Cataract, Alopecia, Sclerodactyly
- Cataract, autosomal dominant
- Cataract, autosomal dominant, multiple types 1
- Cataract, Autosomal Recessive Congenital 2
- Cataract, autosomal recessive congenital 4
- Cataract, congenital nuclear, autosomal recessive 2
- Cataract, congenital nuclear, autosomal recessive 3
- Cataract, congenital zonular, with sutural opacities
- Cataract, congenital, cerulean type, 2
- Cataract, congenital, cerulean type, 3
- Cataract, Congenital, with Microcornea or Slight Microphthalmia
- Cataract, Congenital, with Microphthalmia
- Cataract, congenital, X-linked
- Cataract, coppock-like
- Cataract, cortical, juvenile-onset
- Cataract, crystalline aculeiform
- Cataract, juvenile, with microcornea and glucosuria
- Cataract, lamellar 2
- Cataract, Microphthalmia and Nystagmus
- Cataract, Posterior Polar, 1
- Cataract, posterior polar, 2
- Cataract, Posterior Polar, 3
- Cataract, Posterior Polar, 4
- Cataract, Posterior Polar, 5
- Cataract, pulverulent, juvenile-onset
- Cataract, sutural, with punctate and cerulean opacities
- Cataract, Total Congenital
- Cataract, Zonular
- Cataract, zonular pulverulent 1
- Cataract-Glaucoma
- Cataract-Microcephaly-Failure to Thrive-Kyphoscoliosis
- Cataracts
- Cataracts, Ataxia, Short Stature, and Mental Retardation
- Catastrophic Antiphospholipid Syndrome
- Catatrichy
- Catecholamine Hypertension
- Catecholaminergic polymorphic ventricular tachycardia
- Catel Manzke Syndrome
- CATSPER-related male infertility
- Caudal Duplication
- Caudal Regression
- Caudal Regression Syndrome
- Cavernoma
- Cavernous angioma
- Cavernous hemangioma
- Cavernous Lymphangioma
- Cayler Cardiofacial Syndrome
- CBD
- CCA Syndrome
- CCGE Syndrome
- CCTGA
- CD3 Deficiency
- CD4 Deficiency
- Cd59 deficiency
- CDG 2L
- CDG-x
- CDGS2
- CDK4 Linked Melanoma
- Celiac disease
- Celiac sprue
- Cellulitis
- Central areolar choroidal dystrophy
- Central Auditory Processing Disorder
- Central Core Disease
- Central Nervous System Lymphoma, Primary
- Central Neurocytoma
- Central Pontine Myelinolysis
- Central post-stroke pain
- Central precocious puberty
- Central Serous Chorioretinopathy
- Centromeric Instability Immunodeficiency Syndrome
- Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency
- Centronuclear myopathy
- Centrotemporal Epilepsy
- Ceramide Trihexosidosis
- Cercarial Dermatitis
- Cerebellar Agenesis
- Cerebellar Astrocytoma, Childhood
- Cerebellar Ataxia
- Cerebellar Ataxia Ectodermal Dysplasia
- Cerebellar Ataxia Infantile with Progressive External Ophthalmoplegia
- Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorinural Hearing Loss
- Cerebellar ataxia, cayman type
- Cerebellar Ataxia, Dominant Pure
- Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3
- Cerebellar Degeneration
- Cerebellar Degeneration, Subacute
- Cerebellar Hypoplasia
- Cerebellar Hypoplasia Tapetoretinal Degeneration
- Cerebellar Hypoplasia with Endosteal Sclerosis
- Cerebellar Liponeurocytoma
- Cerebellar Parenchymal Degeneration
- Cerebello-oculo-renal syndrome
- Cerebelloolivary Atrophy
- Cerebelloparenchymal Disorder 3
- Cerebellotrigerminal dermal dysplasia
- Cerebellum Agenesis Hydrocephaly
- Cerebellum Defects
- Cerebral amyloid angiopathy, APP-related
- Cerebral Aneurysm
- Cerebral Astrocytoma, Childhood
- Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Cerebral Calcification Cerebellar Hypoplasia
- Cerebral Calcifications Opalescent Teeth Phosphaturia
- Cerebral cavernous malformation (CCM)
- Cerebral cavernous malformations 1
- Cerebral cavernous malformations 2
- Cerebral cavernous malformations 3
- Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma Syndrome
- Cerebral folate transport deficiency
- Cerebral Gigantism Jaw Cysts
- Cerebral Palsy
- Cerebral Palsy Ataxic
- Cerebral Palsy Athetoid
- Cerebral Palsy Mixed
- Cerebral Palsy Spastic Diplegic
- Cerebral Palsy Spastic Hemiplegic
- Cerebral Palsy Spastic Monoplegic
- Cerebral Palsy Spastic Quadriplegic
- Cerebral Poliodystrophy
- Cerebral sarcoma
- Cerebral Sclerosis Similar to Pelizaeus-Merzbacher Disease
- Cerebral Ventricle Cancer
- Cerebro Facio Thoracic Dysplasia
- Cerebro Oculo Dento Auriculo Skeletal Syndrome
- Cerebro-Costo-Mandibular Syndrome
- Cerebro-Oculo-Facio-Skeletal Syndrome
- Cerebrooculofacioskeletal syndrome 2
- Cerebrooculofacioskeletal syndrome 4
- Cerebroretinal microangiopathy with calcifications and cysts
- Cerebrospinal Fluid Leak
- Cerebrotendinous Xanthomatosis
- Ceroid Lipofuscinosis Neuronal 1
- Ceroid Lipofuscinosis Neuronal 10
- Ceroid Lipofuscinosis Neuronal 2
- Ceroid Lipofuscinosis Neuronal 3
- Ceroid Lipofuscinosis Neuronal 4A Autosomal Recessive
- Ceroid Lipofuscinosis Neuronal 4B Autosomal Dominant
- Ceroid Lipofuscinosis Neuronal 5
- Ceroid Lipofuscinosis Neuronal 6
- Ceroid Lipofuscinosis Neuronal 7
- Ceroid Lipofuscinosis Neuronal 8
- Ceroid Lipofuscinosis Neuronal 9
- Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant
- Cerulean Cataract
- Cervical cancer
- Cervical dysplasia
- Cervical Dystonia
- Cervical Hypertrichosis Neuropathy
- Cervical intraepithelial neoplasia
- Cervical Ribs Sprengel Anomaly Anal Atresia Urethral Obstruction