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Orphanet classification of rare neoplastic diseases

Rare neoplastic disease ORPHA:250908
- Inherited cancer-predisposing syndrome ORPHA:140162
  - Polymalformative genetic syndrome with increased risk of developing cancer ORPHA:183422
    - Aicardi syndrome ORPHA:50
    - Alagille syndrome ORPHA:52
    - Ataxia-telangiectasia ORPHA:100
    - Ataxia-telangiectasia-like disorder ORPHA:251347
    - Bazex syndrome ORPHA:166113
    - Beckwith-Wiedemann syndrome ORPHA:116
    - Bloom syndrome ORPHA:125
    - Cernunnos-XLF deficiency ORPHA:169079
    - Cockayne syndrome ORPHA:191
    - Costello syndrome ORPHA:3071
    - Denys-Drash syndrome ORPHA:220
    - Diamond-Blackfan anemia ORPHA:124
    - Fanconi anemia ORPHA:84
    - Frasier syndrome ORPHA:347
    - Isolated hemihyperplasia ORPHA:2128
    - LIG4 syndrome ORPHA:99812
    - McCune-Albright syndrome ORPHA:562
    - Megalencephaly-capillary malformation-polymicrogyria syndrome ORPHA:60040
    - Mosaic variegated aneuploidy syndrome ORPHA:1052
    - Nijmegen breakage syndrome ORPHA:647
    - Nijmegen breakage syndrome-like disorder ORPHA:240760
    - Noonan syndrome ORPHA:648
    - Noonan syndrome-like disorder with juvenile myelomonocytic leukemia ORPHA:363972
    - Noonan syndrome with multiple lentigines ORPHA:500
    - N syndrome ORPHA:2608
    - Oligodontia-cancer predisposition syndrome ORPHA:300576
    - PCNA-related progressive neurodegenerative photosensitivity syndrome ORPHA:438134
    - Perlman syndrome ORPHA:2849
    - Peutz-Jeghers syndrome ORPHA:2869
    - PTEN hamartoma tumor syndrome ORPHA:306498
    - Rothmund-Thomson syndrome type 2 ORPHA:221016
    - Rubinstein-Taybi syndrome ORPHA:783
    - Saethre-Chotzen syndrome ORPHA:794
    - Schinzel-Giedion syndrome ORPHA:798
    - Schöpf-Schulz-Passarge syndrome ORPHA:50944
    - Shwachman-Diamond syndrome ORPHA:811
    - Silver-Russell syndrome ORPHA:813
    - Simpson-Golabi-Behmel syndrome ORPHA:373
    - Sotos syndrome ORPHA:821
    - Tuberous sclerosis complex ORPHA:805
    - Tyrosinemia type 1 ORPHA:882
    - WAGR syndrome ORPHA:893
    - Warsaw breakage syndrome ORPHA:280558
    - Werner syndrome ORPHA:902
    - Wiskott-Aldrich syndrome ORPHA:906
    - Xeroderma pigmentosum ORPHA:910
    - Xeroderma pigmentosum-Cockayne syndrome complex ORPHA:220295
    - Xeroderma pigmentosum variant ORPHA:90342

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