[Renal cancer and hereditary diseases].

Diseases presenting "early diagnosis" symptom

• achondroplasia

• acute rheumatic fever

• adrenal incidentaloma

• adrenomyeloneuropathy

• alexander disease

• allergic bronchopulmonary aspergillosis

• aromatase deficiency

• carcinoma of the gallbladder

• cholangiocarcinoma

• classical phenylketonuria

• coats disease

• cohen syndrome

• congenital adrenal hyperplasia

• congenital diaphragmatic hernia

• congenital toxoplasmosis

• cowden syndrome

• cushing syndrome

• cutaneous mastocytosis

• cystinuria

• dentin dysplasia

• dentinogenesis imperfecta

• dracunculiasis

• erdheim-chester disease

• erythropoietic protoporphyria

• esophageal carcinoma

• esophageal squamous cell carcinoma

• fabry disease

• familial hypocalciuric hypercalcemia

• familial mediterranean fever

• gm1 gangliosidosis

• hirschsprung disease

• holt-oram syndrome

• homocystinuria without methylmalonic aciduria

• hydrocephalus with stenosis of the aqueduct of sylvius

• inclusion body myositis

• kabuki syndrome

• kallmann syndrome

• kindler syndrome

• krabbe disease

• locked-in syndrome

• monosomy 21

• neuralgic amyotrophy

• oculocutaneous albinism

• oligodontia

• omenn syndrome

• oral submucous fibrosis

• papillon-lefèvre syndrome

• phenylketonuria

• primary effusion lymphoma

• primary hyperoxaluria type 1

• proteus syndrome

• pyomyositis

• pyruvate dehydrogenase deficiency

• scrub typhus

• severe combined immunodeficiency

• sneddon syndrome

• systemic capillary leak syndrome

• thoracic outlet syndrome

• triple a syndrome

• typhoid

• von hippel-lindau disease

• wiskott-aldrich syndrome

• wolf-hirschhorn syndrome