Catalog
Inherited cancer-predisposing syndromes
No MMS code
Link to WHO Definition
Inherited cancer-predisposing syndromes – http://id.who.int/icd/entity/264268169
Parents
Children
- Hashimoto-Pritzker syndrome
- LD2D.4 Gorlin syndrome
- Nijmegen breakage syndrome-like disorder
- Juvenile gastrointestinal polyposis
- LD2F.15 Noonan syndrome
- Oligodontia - cancer predisposition syndrome
- Blue rubber bleb naevus syndrome
- Hemihypertrophy
- Cockayne syndrome
- LD27.1 Xeroderma pigmentosum
- Alagille syndrome
- 2C65 Hereditary breast and ovarian cancer syndrome
- Hereditary breast cancer
- McCune-Albright syndrome
- Enchondromatosis
- Hyperplastic polyposis syndrome
- Blackfan-Diamond anaemia
- Familial platelet syndrome with predisposition to acute myelogenous leukaemia
- Macrocephaly - capillary malformation
- LD2D.11 Neurofibromatosis type 2
- Familial ovarian cancer
- Familial adenomatous polyposis
- Fanconi anaemia
- Dyskeratosis congenita
- Schinzel-Giedion syndrome
- Multiple endocrine neoplasia type 4
- Familial prostate cancer
- Familial multiple meningioma
- Multiple endocrine neoplasia type 1
- Wiskott-Aldrich syndrome
- Simpson-Golabi-Behmel syndrome
- Deafness, lymphoedema and leukaemia syndrome
- Multiple endocrine neoplasia type 2
- Bloom syndrome
- WAGR syndrome
- Werner syndrome
- Sotos syndrome
- LD2D.2 Tuberous sclerosis
- Common variable immunodeficiency
- Nijmegen breakage syndrome
- Costello syndrome
- Li-Fraumeni syndrome
- Von Hippel-Lindau disease
- Cowden syndrome
- 5C50.11 Tyrosinaemia type 1
- N syndrome
- Aicardi syndrome
- Saethre-Chotzen syndrome
- Rothmund-Thomson syndrome type 2
- Ataxia-telangiectasia
- Hereditary mixed polyposis syndrome
- Shwachman-Diamond syndrome
- Ataxia-telangiectasia-like disorder
- Nonpolyposis Turcot syndrome
- LD2D.10 Neurofibromatosis type 1
- Bannayan-Riley-Ruvalcaba syndrome
- Mosaic variegated aneuploidy syndrome
- Bazex-Dupré-Christol syndrome
- Kostmann syndrome
- Birt-Hogg-Dubé syndrome
- Schöpf-Schulz-Passarge syndrome
- Familial renal cell carcinoma
- Familial nonpolyposis colorectal cancer
- Rubinstein-Taybi syndrome
- Silver-Russell syndrome
- Perlman syndrome
- Beckwith-Wiedemann syndrome
- Warsaw breakage syndrome
- Denys-Drash syndrome
- LD2D.12 Neurofibromatosis type 3
- LD2D.0 Peutz-Jeghers syndrome