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17101 to 17200 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Primary Ciliary Dyskinesia 7
Membranoproliferative Glomerulonephritis
Yakut Short-Stature Syndrome
Christianson Syndrome
Acute Prostatitis
X-Linked Hypospadias 1
X-Linked Scapuloperoneal Myopathy
Bone Metastasis
X-Linked Myopathy with Postural Muscle Atrophy
X-Linked Syndromic Mental Retardation Type Wu
X-Linked Spinocerebellar Ataxia Type 5
Urinary Retention
Cranio-Facio-Skeletal Syndrome
X-Linked Reducing-Body Myopathy 1A
Vocal Cord Paralysis
Deafness - Cataract - Retinitis pigmentosa - Sperm Abnormalities
X-Linked Syndromic Mental Retardation Type Najm
X-Linked Spastic Paraplegia Type 34
Parathyroid Carcinoma
X-Linked Erythropoietic Protoporphyria
Camptodactyly Syndrome Type Guadalajara III
Catecholaminergic Polymorphic Ventricular Tachycardia Type 2
Lymphatic Malformation Type 2
Stevenson Carey Syndrome
Biliary Tract Hemorrhage
Hunter-MacDonald Syndrome
Pulmonary Infarction
Thrombocytopenia Type 4
Primary Coenzyme Q10 Deficiency Type 4
Autosomal Recessive Spastic Paraplegia Type 39
Optic Papillitis
Lumbar Spinal Stenosis
Hypocalcemia
Amyotrophic Lateral Sclerosis Type 10
Urethral Syndrome
Secondary Biliary Cirrhosis
ANE Syndrome
Gallbladder Perforation
Hypophosphatemic Rickets and Hyperparathyroidism
Abscess of Salivary Gland
Retinitis Pigmentosa 41
Hypertrophy of Nasal Turbinates
Reactive Depression
Otosclerosis 8
Acute Laryngitis and/or Tracheitis
Unilateral Deafness with Delayed Endolymphatic Hydrops
Degenerative Brain Disorder
Familial Hypertrophic Cardiomyopathy Type 11
Pancreatic Insufficiency
Pancreatic Adenocarcinoma
Familial Hypertrophic Cardiomyopathy Type 12
Epidermolysis Bullosa-Pyloric Atresia
Early Infantile Epileptic Encephalopathy Type 4
Cul De Sac Mass
Retinitis Pigmentosa 29
Diastasis Recti and Weakness of the Linea Alba
Coats Plus Syndrome
Familial Atrial Fibrillation 6
Ascites
Hypomyelinating Leukodystrophy Type 4
Autoimmune Hemolytic Anemia
Familial Atrial Fibrillation 7
Autosomal Recessive Congenital Ichthyosis Type 6
Joubert Syndrome Type 9
Ovarian Pregnancy
Riedel Thyroiditis
Ectopic Pregnancy
Dominant Hypophosphatemia with Nephrolithiasis or Osteoporosis
Ovarian Adenoma
Female Genital Cancer
Ovarian Cyst Torsion
Primary CD59 Deficiency
Galactocele
Ovarian Cyst
Talipes Calcaneovalgus
Tubo-Ovarian Abscess
Secondary Aldosteronism
Autosomal Dominant Spastic Paraplegia Type 38
Ehlers-Danlos Syndrome Spondylodysplastic Type 3
Adenocarcinoma of the Ovary
Pontocerebellar Hypoplasia Type 2B
Pathological Fracture
Connective Tissue Disorder due to Lysyl Hydroxylase-3 Deficiency
Endometriosis
Hypermobility Syndrome
Hypomyelinating Leukodystrophy Type 6
Tendon Rupture
4H Syndrome
Skeletal Defects, Genital Hypoplasia, and Mental Retardation
Adenocarcinoma of the Prostate
Diamond-Blackfan Anemia Type 1
Essential Tremor
2p15-p16.1 Deletion Syndrome
Psychogenic Pruritus
Amelogenesis Imperfecta Type 2A2
Muscle Rupture
Gastropathy
Familial Adenomatous Polyposis
Dyschromatosis Universalis Hereditaria 1
Autosomal Dominant Spastic Paraplegia Type 42