Cutaneous mastocytosis in twins: multiple mastocytomas and urticaria pigmentosa in two pairs of monozygotic twins.

Diseases presenting "first report" symptom

• achondroplasia

• alexander disease

• aniridia

• cadasil

• canavan disease

• child syndrome

• cohen syndrome

• congenital toxoplasmosis

• cowden syndrome

• cushing syndrome

• cutaneous mastocytosis

• cystinuria

• dedifferentiated liposarcoma

• dentinogenesis imperfecta

• dracunculiasis

• dystrophic epidermolysis bullosa

• epidermolysis bullosa simplex

• erdheim-chester disease

• esophageal squamous cell carcinoma

• fabry disease

• familial mediterranean fever

• focal myositis

• harlequin ichthyosis

• hirschsprung disease

• hodgkin lymphoma, classical

• holt-oram syndrome

• homocystinuria without methylmalonic aciduria

• inclusion body myositis

• junctional epidermolysis bullosa

• kabuki syndrome

• kindler syndrome

• krabbe disease

• lamellar ichthyosis

• liposarcoma

• lymphangioleiomyomatosis

• monosomy 21

• neonatal adrenoleukodystrophy

• neuralgic amyotrophy

• oculocutaneous albinism

• oligodontia

• omenn syndrome

• pendred syndrome

• pleomorphic liposarcoma

• primary hyperoxaluria type 1

• pyomyositis

• pyruvate dehydrogenase deficiency

• scrub typhus

• severe combined immunodeficiency

• sneddon syndrome

• triple a syndrome

• typhoid

• waldenström macroglobulinemia

• werner syndrome

• wiskott-aldrich syndrome

• x-linked adrenoleukodystrophy

• zellweger syndrome