Disease Search
- CFD
- CFEOM1B
- CGD
- CGD due to deficiency of the alpha subunit of cytochrome b
- Chagas Disease
- Chanarin-Dorfman Syndrome
- Chancroid
- Chandler's Syndrome
- CHANDS
- Channelopathy-associated congenital analgesia
- Chaotic Atrial Tachycardia
- Char 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 2A
- Charcot-Marie-Tooth Disease Type 2B
- Charcot-Marie-Tooth Disease Type 2C
- 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 4A
- Charcot-Marie-Tooth Disease Type 4B
- Charcot-Marie-Tooth Disease Type 4C
- Charcot-Marie-Tooth Disease Type 4E
- Charcot-Marie-Tooth Disease Type X
- CHARGE association
- CHARGE Syndrome
- Charles Bonnet Syndrome
- CHDH1
- Chediak-Higashi Syndrome
- Cheilitis Glandularis
- Chemical conjunctivitis
- Chemical Porphyria
- Cherubism
- Chest pain
- Chester Porphyria
- Chiari malformation type 1
- Chiari Malformation Type 2
- Chiari Malformation Type 3
- Chiari Malformation Type 4
- Chiari malformations
- Chiari-Frommel Syndrome
- Chikungunya
- Chilaiditi Syndrome
- Chilblain lupus 2
- Chilblain lupus erythematosus
- CHILD Syndrome
- Childhood apraxia of speech
- Childhood atypical hemolytic uremic syndrome
- Childhood autism
- Childhood Cancer
- Childhood Disintegrative Disorder
- Childhood schizophrenia
- Childhood SLE
- Childhood systemic lupus erythematosus
- Childhood-onset cerebral adrenoleukodystrophy
- Chitotriosidase deficiency
- Chitty Hall Baraitser Syndrome
- Chlamydia
- CHMP2B frontotemporal dementia
- Choanal atresia and lymphedema
- Cholecystitis
- Choledochal cysts
- Cholelithiasis
- Cholelithiasis with ABCB4 gene mutation
- Cholelithiasis:low phospholipid associated
- Cholera
- Cholestanol storage disease
- Cholestasis
- Cholestasis of pregnancy
- Cholestasis Pigmentary Retinopathy Cleft Palate
- Cholestasis, Intrahepatic of Pregnancy
- Cholestasis, Progressive Familial Intrahepatic 1
- Cholestasis, Progressive Familial Intrahepatic 2
- Cholestasis, Progressive Familial Intrahepatic 3
- Cholestatic Jaundice Renal Tubular Insufficiency
- Cholesteatoma
- Cholesterol monooxygenase (side-chain cleaving) deficiency
- Cholesterol Pneumonia
- Cholesterol-ester transfer protein deficiency
- Cholesteryl ester storage disease
- Chondroblastoma
- Chondrocalcinosis
- Chondrocalcinosis 1
- Chondrocalcinosis 2
- Chondrocalcinosis due to Apatite Crystal Deposition
- Chondrodysplasia Acromesomelic with Genital Anomalies
- Chondrodysplasia Blomstrand Type
- Chondrodysplasia Calcificans Metaphysealis
- Chondrodysplasia lethal recessive
- Chondrodysplasia Pseudohermaphrodism Syndrome
- Chondrodysplasia Punctata 1, X-Linked Recessive
- Chondrodysplasia Punctata 2 X-Linked Dominant
- Chondrodysplasia punctata Sheffield type
- Chondrodysplasia Punctata Syndrome
- Chondrodysplasia with joint dislocations, gpapp type
- Chondrodysplasia, Grebe Type
- Chondroectodermal dysplasia
- Chondroma
- Chondromalacia patellae
- Chondrosarcoma
- Chordoid glioma of the third ventricle
- Chordoma
- Chorea Familial Benign
- Chorea minor
- Chorea, Remitting with Nystagmus and Cataracts
- Choreoacanthocytosis
- Choreoathetosis, hypothyroidism, and neonatal respiratory distress
- Chorioblastoma
- Choriocarcinoma
- Chorioretinal Atrophy, Progressive Bifocal
- Chorioretinitis
- Chorioretinopathy dominant form microcephaly
- Choroid Plexus Calcification with Mental Retardation
- Choroid plexus carcinoma
- Choroid plexus cyst
- Choroid Plexus Papilloma
- Choroid plexus tumor
- Choroideremia
- Choroiditis
- Christ-Siemens-Touraine syndrome
- Christianson Syndrome
- Christmas disease
- CHRNA1-related congenital myasthenic syndrome
- CHRNB2-Related Nocturnal Frontal Lobe Epilepsy, Autosomal Dominant
- Chrombolastomycosis
- Chromomycosis
- Chromophil Renal Cell Carcinoma
- Chromophobe renal cell carcinoma
- Chromosomal Triplication
- Chromosome 1, Deletion q21 q25
- Chromosome 1, monosomy 1p
- Chromosome 1, Monosomy 1p22 p13
- Chromosome 1, q42 11 q42 12 Duplication
- Chromosome 1, Trisomy 1q32 qter
- Chromosome 1, Trisomy 1q42-qter
- Chromosome 10, Distal Trisomy 10q
- Chromosome 10, Monosomy 10p
- Chromosome 10, Monosomy 10q
- Chromosome 10, Ring
- Chromosome 10, Trisomy 10p
- Chromosome 10p Terminal Deletion Syndrome
- Chromosome 11, Partial Trisomy 11q
- Chromosome 11p11.2 deletion syndrome
- Chromosome 11p13 deletion syndrome
- Chromosome 11q Partial Deletion
- Chromosome 12, 12p Trisomy
- Chromosome 12, Ring
- Chromosome 12, Trisomy 12q
- Chromosome 12p Partial Deletion
- Chromosome 13, Partial Monosomy 13q
- Chromosome 13, Ring
- Chromosome 13p Duplication
- Chromosome 13q Deletion
- Chromosome 13q Trisomy
- Chromosome 14 Deletion
- Chromosome 14 Trisomy
- Chromosome 14, Deletion 14q, Partial Duplication 14p
- Chromosome 14, Ring
- Chromosome 14, Trisomy Mosaic
- Chromosome 14;16 Translocation
- Chromosome 14q, Partial Deletions
- Chromosome 14q, Proximal Duplication
- Chromosome 14q, Terminal Deletion
- Chromosome 14q, Terminal Duplication
- Chromosome 15 Ring
- Chromosome 15, Distal Trisomy 15q
- Chromosome 15, Trisomy Mosaicism
- Chromosome 15q Duplication Mosaicism
- Chromosome 15q Duplications
- Chromosome 15q, Partial Deletion
- Chromosome 15q, Tetrasomy
- Chromosome 15q, Trisomy
- Chromosome 16
- Chromosome 16, Ring
- Chromosome 16, Trisomy
- Chromosome 16, Trisomy 16p
- Chromosome 16, Uniparental Disomy
- Chromosome 16q, Trisomy
- Chromosome 17, Deletion
- Chromosome 17, Deletion 17q23 q24
- Chromosome 17, Duplication
- Chromosome 17, Ring
- Chromosome 17, Trisomy 17p
- Chromosome 17, Trisomy 17p11 2
- Chromosome 17, Trisomy 17q22
- Chromosome 17, Trisomy Mosaicism
- Chromosome 17p13.1 deletion syndrome
- Chromosome 18
- Chromosome 18 Deletion Syndrome
- Chromosome 18 Mosaic Monosomy
- Chromosome 18 Translocations
- Chromosome 18, Deletion 18q23
- Chromosome 18, Ring
- Chromosome 18, Tetrasomy 18p
- Chromosome 18, Trisomy 18p
- Chromosome 18, Trisomy 18q
- Chromosome 18p Deletion Syndrome
- Chromosome 18p duplication
- Chromosome 18p tetrasomy
- Chromosome 18p-
- Chromosome 18q-
- Chromosome 19 Ring Syndrome
- Chromosome 19, Ring
- Chromosome 19, Trisomy 19q
- Chromosome 19q13.11 Deletion Syndrome
- Chromosome 1p36 Deletion Syndrome
- Chromosome 1q Deletion
- Chromosome 1q, Duplication 1q12 q21
- Chromosome 1q21.1 Duplication Syndrome
- Chromosome 1q41-q42 deletion syndrome
- Chromosome 2 Duplication
- Chromosome 2 Duplication Disease
- Chromosome 2, Duplication(2)(p13)(p21)
- Chromosome 2, Monosomy 2p22
- Chromosome 2, Monosomy 2pter p24
- Chromosome 2, Monosomy 2q
- Chromosome 2, Monosomy 2q24
- Chromosome 2, Monosomy 2q37
- Chromosome 2, Trisomy 2pter p24
- Chromosome 2, Trisomy 2q
- Chromosome 2, Trisomy 2q37
- Chromosome 20 Ring
- Chromosome 20, Deletion 20p
- Chromosome 20, Duplication 20p
- Chromosome 20, Trisomy
- Chromosome 21 Monosomy
- Chromosome 21 Ring
- Chromosome 21, Monosomy 21q22
- Chromosome 21, Tetrasomy 21q
- Chromosome 21, Uniparental Disomy Of
- Chromosome 22
- Chromosome 22 Ring
- Chromosome 22 Trisomy Mosaic
- Chromosome 22, Monosome Mosaic
- Chromosome 22, Trisomy
- Chromosome 22, Trisomy q11 q13
- Chromosome 22q
- Chromosome 22q Deletion
- Chromosome 2p Duplication
- CHROMOSOME 2q23.1 DELETION SYNDROME
- Chromosome 2q37 deletion syndrome
- Chromosome 3 Duplication Syndrome
- Chromosome 3, Monosomy 3p
- Chromosome 3, Monosomy 3p14 p11
- Chromosome 3, Monosomy 3p2
- Chromosome 3, Monosomy 3p25
- Chromosome 3, Monosomy 3q13
- Chromosome 3, Monosomy 3q21 23
- Chromosome 3, Monosomy 3q27
- Chromosome 3, Trisomy 3p
- Chromosome 3, Trisomy 3p25
- Chromosome 3, Trisomy 3q
- Chromosome 3, Trisomy 3q13 2 q25
- Chromosome 3, Trisomy 3q2
- Chromosome 3p duplication
- Chromosome 3q29 Microduplication Syndrome
- Chromosome 4 Ring Syndrome
- Chromosome 4 Short Arm Deletion
- Chromosome 4, Monosomy 4p14 p16
- Chromosome 4, Monosomy 4q
- Chromosome 4, Monosomy 4q32
- Chromosome 4, Monosomy Distal 4q
- Chromosome 4, Partial Trisomy Distal 4q
- Chromosome 4, Trisomy 4p
- Chromosome 4, Trisomy 4q
- Chromosome 4, Trisomy 4q21
- Chromosome 4, Trisomy 4q25 qter
- Chromosome 5, Monosomy 5q35
- Chromosome 5, Trisomy 5p
- Chromosome 5, Trisomy 5pter p13 3
- Chromosome 5, Trisomy 5q
- Chromosome 5, Uniparental disomy
- Chromosome 5p deletion syndrome
- Chromosome 5p duplication
- Chromosome 5p-
- Chromosome 5p- syndrome
- Chromosome 5q14.3 deletion syndrome
- Chromosome 6 Ring Syndrome
- Chromosome 6, Deletion 6q13 q15
- Chromosome 6, Monosomy 6p23
- Chromosome 6, Monosomy 6q
- Chromosome 6, Monosomy 6q1
- Chromosome 6, Monosomy 6q2
- Chromosome 6, Partial Trisomy 6q
- Chromosome 6, Trisomy 6p
- Chromosome 6, Trisomy 6q
- Chromosome 6q24-q25 deletion syndrome
- Chromosome 7 Ring Syndrome
- Chromosome 7, Monosomy
- Chromosome 7, Monosomy 7q2
- Chromosome 7, Monosomy 7q21
- Chromosome 7, Monosomy 7q3
- Chromosome 7, Partial Monosomy 7p
- Chromosome 7, Terminal Deletion, 7q36
- Chromosome 7, Trisomy 7p
- Chromosome 7, Trisomy 7p13 p12 2
- Chromosome 7, Trisomy 7q
- Chromosome 7, Trisomy Mosaic
- Chromosome 8 Deletion
- Chromosome 8 Ring
- Chromosome 8, Monosomy 8p
- Chromosome 8, Monosomy 8p2
- Chromosome 8, Monosomy 8p23 1
- Chromosome 8, Monosomy 8q
- Chromosome 8, Mosaic Trisomy
- Chromosome 8, Partial Trisomy
- Chromosome 8, Trisomy
- Chromosome 8, Trisomy 8p
- Chromosome 8, Trisomy 8q
- Chromosome 8p
- Chromosome 9
- Chromosome 9 inversion
- Chromosome 9 Inversion or Duplication
- Chromosome 9 Ring
- Chromosome 9, Deletion 9q21.33q22.32
- Chromosome 9, Duplication 9q21
- Chromosome 9, Monosomy 9p
- Chromosome 9, Partial Monosomy 9p
- Chromosome 9, Partial Trisomy 9p
- Chromosome 9, Tetrasomy 9p
- Chromosome 9, Trisomy
- Chromosome 9, Trisomy 9p
- Chromosome 9, Trisomy 9q
- Chromosome 9, Trisomy 9q32
- Chromosome 9, Trisomy Mosaic
- Chromosome 9p-
- Chromosome 9q deletion syndrome
- Chromosome 9q Duplication
- Chromosome Anomalies
- Chromosome Deletions
- Chromosome Duplications
- Chromosome Inversions
- Chromosome Mosaicism
- Chromosome Translocations
- Chromosome Two Duplication
- Chromosome Two Duplication Syndrome
- Chronic Berylliosis
- Chronic bronchitis
- Chronic Demyelinizing Neuropathy with IgM Monoclonal
- Chronic depression
- Chronic disability
- Chronic Erosive Gastritis
- Chronic fatigue syndrome
- Chronic Functional Abdominal Pain
- Chronic Graft versus Host Disease
- Chronic Granulomatous Disease
- Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type I
- Chronic granulomatous disease, autosomal recessive cytochrome b-positive, type II
- Chronic granulomatous disease, x-linked
- Chronic Hiccup
- Chronic illness
- Chronic infantile neurological cutaneous articular syndrome
- Chronic Inflammatory Demyelinating Polyneuropathy
- Chronic kidney disease
- Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
- Chronic Lymphocytic Leukemia
- Chronic mucocutaneous candidiasis familial
- Chronic Myeloid Leukemia
- Chronic Myelomonocytic Leukemia
- Chronic Myeloproliferative Disorders
- Chronic Necrotizing Vasculitis
- Chronic Neutrophilic Leukemia
- Chronic obstructive pulmonary disease
- Chronic Polyradiculoneuritis
- Chronic Progressive External Ophthalmoplegia
- Chronic Recurrent Multifocal Osteomyelitis
- Chudley Rozdilsky Syndrome
- Chudley-Mccullough Syndrome
- Churg-Strauss Syndrome
- Chuvash erythrocytosis
- Chuvash polycythemia
- Chylomicron Retention Disease
- Chylomicron Retention Disease (CMRD)
- Chylothorax, Congenital
- Chylous Ascites
- Cicatricial Pemphigoid
- Ciguatera Fish Poisoning
- Ciliary Discoordination, due to Random Ciliary Orientation
- Ciliary Dyskinesia with Excessively Long Cilia
- Ciliary Dyskinesia, due to Transposition of Ciliary Microtubules
- Ciliary dyskinesia, primary, 10
- Ciliary dyskinesia, primary, 11
- Ciliary dyskinesia, primary, 12
- Ciliary dyskinesia, primary, 13
- Ciliary dyskinesia, primary, 14
- Ciliary dyskinesia, primary, 15
- Ciliary dyskinesia, primary, 16
- Ciliary dyskinesia, primary, 2
- Ciliary dyskinesia, primary, 3
- Ciliary dyskinesia, primary, 6
- Ciliary dyskinesia, primary, 7
- Ciliary dyskinesia, primary, 9
- Ciliary Dyskinesia-Bronchiectasis
- Cilliers Beighton Syndrome
- CINCA
- Circumscribed Cutaneous Aplasia of the Vertex
- Cirrhosis of the Liver
- Citrin Deficiency
- Citrulline Transport Defect
- Citrullinemia type I
- Citrullinemia type II
- CJD