Increased risk of neoplasm

May Be Caused by
Abdominal compartment syndrome
Achondroplasia
Adrenal hyperplasia
Adrenogenital syndrome
AIDS
Alagille syndrome
Albinism
Alpha1-antitrypsin deficiency
Alport syndrome
Aniridia
Asphyxiating thoracic dysplasia
Ataxia-telangiectasia
Bannayan-Riley-Ruvalcaba syndrome
Basaloid follicular hamartoma
Bazex syndrome
Beckwith-Wiedemann syndrome
Behçet disease
Birt-Hogg-Dubé syndrome
Bloom syndrome
Blue rubber bleb nevus syndrome
Carcinoid syndrome
Carney complex
Carney triad
Castleman disease
Celiac disease
Chédiak-Higashi syndrome
Clark-Howel-Evans-McConnell syndrome
Costello syndrome
Cowden syndrome
Cronkhite-Canada syndrome
De Sanctis-Cacchione syndrome
Diamond-Blackfan syndrome
Disorganization complex
Doege-Potter syndrome
Dubowitz syndrome
Dyskeratosis congenita
Ehlers-Danlos syndrome
Enchondromatosis
Epidermal nevus syndrome
Epidermolysis bullosa
Familial adenomatous polyposis
Fanconi anemia
Fanconi syndrome
Fetal alcohol syndrome
Fetal hydantoin syndrome
Fibrous dysplasia
Frasier syndrome
Galactosemia
Gardner syndrome
Glucagonoma syndrome
Glycogen storage disease type 1
Gorlin syndrome
Hardcastle syndrome
Hemihypertrophy
Hemochromatosis
Henoch-Schönlein purpura
Hepatic fibrosis-renal cystic disease
Hereditary multiple exostosis
Hereditary nonpolyposis colon cancer
Hyperparathyroidism-jaw tumor syndrome
Hyperphenylalaninemia
Incontinentia pigmenti
Kasabach-Merritt syndrome
Klinefelter syndrome
Lambert-Eaton syndrome
Li-Fraumeni cancer family syndrome
Littoral cell angioma
Lynch syndrome
Maffucci syndrome
Male pseudohermaphroditism
Marfan syndrome
Mazabraud syndrome
Meigs syndrome
Melorheostosis
Metachondromatosis
Metaphyseal chondrodysplasia Shwachman type
Mirizzi syndrome
MSH6 mutation
Muir-Torre syndrome
Multiple endocrine neoplasia syndrome type 1
Multiple endocrine neoplasia syndrome type 2A
Multiple endocrine neoplasia syndrome type 2B
Myasthenic syndrome
N syndrome
Nephrogenic hepatic dysfunction syndrome
Nephrotic syndrome
Neurocutaneous melanosis sequence
Neurofibromatosis type 1
Neurofibromatosis type 2
Niemann-Pick disease
Nijmegen breakage syndrome
Oculo-auriculo-vertebral spectrum
Oral leukoplakia associated with tylosis and esophageal carcinoma
OSLAM syndrome
Osteogenesis imperfecta
Osteopetrosis
Osteopoikilosis
Paget disease of bone
Pallister-Hall syndrome
Paraneoplastic syndrome
Perlman syndrome
Persistent müllerian duct syndrome
Peutz-Jeghers syndrome
Pleuropulmonary blastoma-Wilms tumor association
Poland syndrome
Polyostotic fibrous dysplasia
Porphyria cutanea tarda
Richter syndrome
Ring chromosome 13
Rothmund-Thomson syndrome
Rubinstein-Taybi syndrome
Sjögren syndrome
Sotos syndrome
Spondyloepiphyseal dysplasia tarda
Sterno-costo-clavicular hyperostosis
Stewart-Treves syndrome
Sweet syndrome
Syndrome of inappropriate secretion of antidiuretic hormone
Thymic tumor syndrome
Trisomy 21
Trousseau syndrome
Tuberous sclerosis
Tumor lysis syndrome
Turcot syndrome
Turner syndrome
Tyrosinemia
Vasculopathy
Von Hippel-Lindau disease
WAGR syndrome
Weinberg-Zumwalt syndrome
Werner syndrome
Wilms tumor-multiple lung hamartomas
Wiskott-Aldrich syndrome
WT limb-blood syndrome
X-linked lymphoproliferative syndrome
Xeroderma pigmentosa syndrome
Yellow nail syndrome
Zollinger-Ellison syndrome

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