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17301 to 17400 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Malignant Pericardial Effusion
Familial Progressive Cardiac Conduction Defect
Choreoathetosis - Hypothyroidism - Neonatal Respiratory Distress
Dermatomyositis
Frontal Lobe Neoplasm
Autosomal Recessive Deafness 24
Toxocariasis
Syndrome of Inappropriate Antidiuretic Hormone Secretion
Exposure to Toxin
Hypercalcemia
Tobacco Use Disorder
Metastatic Skin Carcinoma
Distal Spinal Muscular Atrophy Type 4
Tobacco
Disseminated Intravascular Coagulation
Autosomal Recessive Mental Retardation Type 5
Thyrotoxicosis
Metastatic Liver Carcinoma
Thyroiditis
Breast Abscess
Thrombophlebitis
Thrombocytosis
Retinitis Pigmentosa 37
Brachial Plexus Neuropathy
Metastatic Adenocarcinoma of the Breast
Breast Fibroadenoma
Breast Hematoma
Autosomal Dominant Spastic Ataxia Type 1
Fat Necrosis of the Breast
Hamamy Syndrome
Thalassemia
Breast Hamartoma
Charcot-Marie-Tooth Disease Type 4J
Autosomal Recessive Spastic Paraplegia Type 32
Microglandular Adenosis
Fibrocystic Breast Disease
Focal Task Specific Dystonia
Autosomal Recessive Spastic Ataxia Type 2
Carcinoma of the Male Breast
Limb-Girdle Muscular Dystrophy Type 2L
Splenic Metastasis
Testicular Neoplasm
Secondary Syphilis of Skin
Cardiac Metastasis
Mungan Syndrome
Brachydactyly Type B2
Adenocarcinoma of the Breast
Autosomal Recessive Spastic Ataxia with Leukoencephalopathy
Legius Syndrome
Autosomal Dominant Mental Retardation Type 1
Mitochondrial Trifunctional Protein Deficiency
Gastric Dilatation
Bladder Neck Obstruction
Tyrosine Kinase 2 Deficiency
Staphylococcal Infection
Pontocerebellar Hypoplasia Type 6
Spinal Cord Tumor
Somatoform Disorders
Soft Tissue Injury
Bladder Adenocarcinoma
Meckel Syndrome Type 5
Muscular Dystrophy-Dystroglycanopathy Type C4
Lissencephaly due to TUBA1A Mutation
Isolated Autosomal Dominant Preauricular Tag 1
Familial Temporal Lobe Epilepsy Type 3
Gastrointestinal Hemorrhage
Familial Temporal Lobe Epilepsy Type 4
Upper Gastrointestinal Bleeding
Familial Febrile Seizures Type 9
Adult Primary Lateral Sclerosis
Skin Neoplasm
Cholestasis
Lymphadenitis
Infant Acute Respiratory Distress Syndrome
Severe Neonatal-Onset Encephalopathy with Microcephaly
Strain of Adductor Muscle and Tendon
X-Linked Syndromic Mental Retardation Type 13
Spinocerebellar Ataxia Type 10
Hashimoto Thyroiditis
Gaucher Disease Type 1
Neonatal Hypoglycemia
Dihydropyrimidine Dehydrogenase Deficiency
Systemic Scleroderma
Familial Teutschlaender Disease
Neuronal Ceroid Lipofuscinosis Type 2
Limb-Girdle Muscular Dystrophy Type 2A
Paroxysmal Non-Kinesigenic Dyskinesia
Traumatic Rupture
Addisonian Crisis
Ear - Patella - Short Stature Syndrome
Paroxysmal Kinesigenic Dyskinesia
Griscelli Syndrome Type 2
Thanatophoric Dysplasia Type 1
Vitiligo
Autosomal Recessive Juvenile Parkinson Disease
Depression
HIV Wasting Syndrome
Hereditary Early-Onset Parkinson Disease
Chronic Fatigue Syndrome
Perry Syndrome