18701 to 18800 most common queries

List represents a sample of symptoms, diseases, and other queries. Updated weekly.

• Enamel Hypoplasia Cataracts and Aqueductal Stenosis
• Proprotein Convertase 1 Deficiency
• Postoperative Dehiscence
• Thost-Unna Palmoplantar Keratoderma
• Acute Peritonitis
• Multiple Epiphyseal Dysplasia due to Collagen 9 Anomaly
• Intravenous Drugs
• Abarelix
• Familial Hemiplegic Migraine Type 1
• Abacavir
• Anaphylaxis
• Usher Syndrome Type 1D
• Sexual Dysfunction
• Benign Adult Familial Myoclonic Epilepsy
• Intrahepatic Cholestasis
• Toxic Hepatitis
• MURCS Association
• Congenital Disorder of Glycosylation Type 1D
• Drug-induced Cholestatic Hepatitis
• Brachydactyly Type A2
• Epithelial Cyst
• Cholestatic Jaundice
• Autosomal Dominant Spastic Paraplegia Type 9A
• Matthew Wood Syndrome
• Verloes-Bourguignon Syndrome
• Autosomal Dominant Deafness 11
• Alopecia
• CAPOS Syndrome
• Ectodermal Dysplasia with Natal Teeth Type Turnpenny
• Acne Vulgaris
• Martinez-Frias Syndrome
• Yim-Ebbin Syndrome
• Autosomal Dominant Deafness 9
• Priapism
• Charcot-Marie-Tooth Disease Type 4B1
• Peliosis Hepatis
• Cerebro-Facio-Articular Syndrome
• Myofibrillar Myopathy Type 1
• Charcot-Marie-Tooth Disease Type 4D
• 17-Hydroxycorticosteroid
• Hereditary Congenital Facial Paresis Type 1
• Charcot-Marie-Tooth Disease Type 2D
• Congenital Hypotrichosis with Juvenile Macular Dystrophy
• Opitz G/BBB Syndrome Type 2
• Rapp-Hodgkin Syndrome
• Pachyonychia Congenita Type 2
• Hyper-IgM Syndrome Type 5
• Hyper-IgM Syndrome Type 3
• Hyper-IgM Syndrome Type 2
• Congenital Generalized Lipodystrophy Type 2
• Congenital Generalized Lipodystrophy Type 1
• Pachyonychia Congenita Type 1
• Lymphatic Malformation Type 1
• Mayer-Rokitansky-Küster-Hauser Syndrome
• Isolated Ectopia Lentis
• Catecholaminergic Polymorphic Ventricular Tachycardia
• Hereditary Renal Aplasia
• Usher Syndrome 3A
• Autosomal Recessive Alport Syndrome
• Autosomal Dominant Alport Syndrome
• X-Linked Alport Syndrome
• Kallmann Syndrome Type 2
• Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis
• ACys Amyloidosis
• Gorlin Psaume Syndrome
• Retinitis Pigmentosa 23
• Primary Torsion Dystonia 6
• Autosomal Dominant Autoimmune Lymphoproliferative Syndrome Type 1
• Oculootoradial Syndrome
• WT Syndrome
• Revesz Syndrome
• Congenital Vitamin B12 Deficiency
• Congenital Dyserythropoietic Anemia Type 2
• Oguchi Disease
• Developmental Dysplasia of the Hip Type 1
• Nicolaides-Baraitser Syndrome
• Spondyloepimetaphyseal Dysplasia Type SPONASTRIME
• Thanatophoric Dysplasia Type 2
• Ribose-5-Phosphate Isomerase Deficiency
• Aromatic L-Amino Acid Decarboxylase Deficiency
• Beta-Ureidopropionase Deficiency
• Iodide Peroxidase Deficiency
• Platelet-Type von Willebrand Disease
• X-Linked Severe Combined Immunodeficiency
• Epidermolysis Bullosa Pruriginosa
• KID Syndrome
• Glaucoma Related Pigment Dispersion Syndrome
• Congenital Thrombotic Thrombocytopenic Purpura
• Von Willebrand Disease Type 1
• Congenital Muscular Dystrophy Type 1A
• Baraitser Syndrome
• Familial Hyperaldosteronism Type 1
• Infantile Sialic Acid Storage Disease
• Frasier Syndrome
• Familial Infantile Myoclonic Epilepsy
• Hajdu Cheney Syndrome
• Deficiency of Ceruloplasmin
• Danon Disease
• Mitochondrial Neurogastrointestinal Encephalomyopathy
• Calcium Pyrophosphate Arthropathy