Kann verursacht werden durch
- 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-Schonlein 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
- Sjogren 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
Synonyme: