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Hereditary neoplastic syndrome
MONDO:0015356The inherited predisposition toward getting a tumor.
Also known as: cancer syndrome, hereditary, cancer syndromes, hereditary, familial neoplastic syndrome, familial tumor syndrome, familial tumour syndrome, hereditary cancer syndrome, hereditary cancer syndromes, hereditary neoplastic syndrome
734 clinical trials for this condition and its sub-types, 60 tagged with Hereditary neoplastic syndrome itself.
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Sub-types of Hereditary neoplastic syndrome
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Glioma susceptibility 0 trials · 133 incl. sub-types
10 sub-types
- Glioma susceptibility 1 133 trials
- Glioma susceptibility 2 0 trials
- Glioma susceptibility 3 0 trials
- Glioma susceptibility 4 0 trials
- Glioma susceptibility 5 0 trials
- Glioma susceptibility 6 0 trials
- Glioma susceptibility 7 0 trials
- Glioma susceptibility 8 0 trials
- Melanoma, cutaneous malignant, susceptibility to, 9 0 trials
- Tumor predisposition syndrome 3 0 trials
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Neurofibromatosis 19 trials · 94 incl. sub-types
5 sub-types
- Neurofibromatosis type 1 73 trials Sub-types →
- NF2-related schwannomatosis 21 trials
- Schwannomatosis 3 trials Sub-types →
- Neurofibromatosis-Noonan syndrome 2 trials Sub-types →
- Neurofibromatosis, type IV, of Riccardi 0 trials
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Hereditary nonpolyposis colon cancer 5 trials · 88 incl. sub-types
5 sub-types
- Lynch syndrome 81 trials · 83 incl. sub-types Sub-types →
- Muir-Torre syndrome 2 trials
- Colorectal cancer, hereditary nonpolyposis, type 6 1 trial
- Colorectal cancer, hereditary nonpolyposis, type 7 0 trials
- Familial colorectal cancer type X 0 trials
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Multiple endocrine neoplasia 7 trials · 62 incl. sub-types
3 sub-types
- Multiple endocrine neoplasia type 1 34 trials
- Multiple endocrine neoplasia type 2 4 trials · 30 incl. sub-types Sub-types →
- Multiple endocrine neoplasia type 4 0 trials
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Intestinal polyposis syndrome 3 trials · 53 incl. sub-types
8 sub-types
- Classic or attenuated familial adenomatous polyposis 0 trials · 35 incl. sub-types Sub-types →
- Peutz-Jeghers syndrome 9 trials
- Hereditary mixed polyposis syndrome 5 trials · 6 incl. sub-types Sub-types →
- Juvenile polyposis syndrome 5 trials Sub-types →
- Bannayan-Riley-Ruvalcaba syndrome 1 trial
- Cronkhite-Canada syndrome 1 trial
- Hyperplastic polyposis syndrome 1 trial Sub-types →
- Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome 0 trials
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Tuberous sclerosis 41 trials · 44 incl. sub-types
2 sub-types
- Tuberous sclerosis 1 33 trials
- Tuberous sclerosis 2 2 trials
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BRCA2-related cancer predisposition 36 trials · 38 incl. sub-types
3 sub-types
- Breast-ovarian cancer, familial, susceptibility to, 2 2 trials
- Glioma susceptibility 3 0 trials
- Pancreatic cancer, susceptibility to, 2 0 trials
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Hereditary breast ovarian cancer syndrome 35 trials · 38 incl. sub-types
2 sub-types
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Mismatch repair cancer syndrome 1 34 trials
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BRCA1-related cancer predisposition 23 trials · 27 incl. sub-types
2 sub-types
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Li-Fraumeni syndrome 16 trials
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PALB2-related cancer predisposition 14 trials
1 sub-type
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Dyskeratosis congenita 12 trials
16 sub-types
- DKC1-related disorder 0 trials · 3 incl. sub-types Sub-types →
- Revesz syndrome 2 trials
- Dyskeratosis congenita and related telomere biology disorder 1 trial Sub-types →
- Autosomal recessive dyskeratosis congenita 4 0 trials
- Dyskeratosis congenita, autosomal dominant 1 0 trials
- Dyskeratosis congenita, autosomal dominant 2 0 trials
- Dyskeratosis congenita, autosomal dominant 3 0 trials
- Dyskeratosis congenita, autosomal dominant 4 0 trials
- Dyskeratosis congenita, autosomal dominant 6 0 trials
- Dyskeratosis congenita, autosomal recessive 1 0 trials
- Dyskeratosis congenita, autosomal recessive 2 0 trials
- Dyskeratosis congenita, autosomal recessive 3 0 trials
- Dyskeratosis congenita, autosomal recessive 6 0 trials
- Dyskeratosis congenita, autosomal recessive 7 0 trials
- Dyskeratosis congenita, autosomal recessive 8 0 trials
- Dyskeratosis congenita, digenic 0 trials
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Wiskott-Aldrich syndrome 10 trials
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PTEN hamartoma tumor syndrome 6 trials · 8 incl. sub-types
4 sub-types
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CHEK2-related cancer predisposition 7 trials
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Susceptibility to familial cutaneous melanoma 0 trials · 7 incl. sub-types
10 sub-types
- Melanoma, cutaneous malignant, susceptibility to, 2 6 trials
- Melanoma, cutaneous malignant, susceptibility to, 1 1 trial
- Melanoma, cutaneous malignant, susceptibility to, 3 0 trials
- Melanoma, cutaneous malignant, susceptibility to, 4 0 trials
- Melanoma, cutaneous malignant, susceptibility to, 5 0 trials
- Melanoma, cutaneous malignant, susceptibility to, 6 0 trials
- Melanoma, cutaneous malignant, susceptibility to, 7 0 trials
- Melanoma, cutaneous malignant, susceptibility to, 8 0 trials
- Melanoma, cutaneous malignant, susceptibility to, 9 0 trials
- Tumor predisposition syndrome 3 0 trials
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Beckwith-Wiedemann syndrome 6 trials
8 sub-types
- Beckwith-Wiedemann syndrome due to 11p15 microdeletion 0 trials
- Beckwith-Wiedemann syndrome due to 11p15 microduplication 0 trials
- Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion 0 trials
- Beckwith-Wiedemann syndrome due to CDKN1C mutation 0 trials
- Beckwith-Wiedemann syndrome due to NSD1 mutation 0 trials
- Beckwith-Wiedemann syndrome due to imprinting defect of 11p15 0 trials
- Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 0 trials
- Franceschini Vardeu Guala syndrome 0 trials
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RAD51C-related cancer predisposition 6 trials
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9 sub-types
- MAX-related tumor predisposition 0 trials
- TMEM127-related tumor predisposition 0 trials
- Pheochromocytoma/paraganglioma syndrome 1 0 trials
- Pheochromocytoma/paraganglioma syndrome 2 0 trials
- Pheochromocytoma/paraganglioma syndrome 3 0 trials
- Pheochromocytoma/paraganglioma syndrome 4 0 trials
- Pheochromocytoma/paraganglioma syndrome 5 0 trials
- Pheochromocytoma/paraganglioma syndrome 6 0 trials
- Pheochromocytoma/paraganglioma syndrome 7 0 trials
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Nevoid basal cell carcinoma syndrome 5 trials
2 sub-types
- Basal cell nevus syndrome 1 0 trials
- Basal cell nevus syndrome 2 0 trials
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Hereditary thrombocytopenia and hematologic cancer predisposition syndrome 1 trial · 5 incl. sub-types
2 sub-types
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RAD51D-related cancer predisposition 4 trials
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Kostmann syndrome 3 trials
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Li-fraumeni-like syndrome 3 trials
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1 sub-type
- Melanoma-pancreatic cancer syndrome 0 trials
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Hereditary multiple osteochondromas 3 trials
3 sub-types
- Exostoses, multiple, type 1 2 trials
- Exostoses, multiple, type 2 0 trials
- Exostoses, multiple, type III 0 trials
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BARD1-related cancer predisposition 2 trials
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Maffucci syndrome 2 trials
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Blue rubber bleb nevus 2 trials
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Hereditary retinoblastoma 2 trials
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Neuroblastoma, susceptibility to, 3 2 trials
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Brooke-Spiegler syndrome 0 trials · 2 incl. sub-types
2 sub-types
- Familial cylindromatosis 2 trials
- Familial multiple trichoepithelioma 0 trials Sub-types →
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Rothmund-Thomson syndrome 1 trial
4 sub-types
- Rothmund-Thomson syndrome type 1 0 trials
- Rothmund-Thomson syndrome type 2 0 trials
- Rothmund-Thomson syndrome type 3 0 trials
- Rothmund-Thomson syndrome type 4 0 trials
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WAGR syndrome 1 trial
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Cherubism 1 trial
1 sub-type
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Familial rhabdoid tumor 0 trials · 1 incl. sub-types
2 sub-types
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ATM-related cancer predisposition 0 trials
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Carney-Stratakis syndrome 0 trials
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Cobb syndrome 0 trials
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HAVCR2-related cancer predisposition 0 trials
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Kaposi sarcoma, susceptibility to 0 trials
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N syndrome 0 trials
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3 sub-types
- Hyperparathyroidism 1 0 trials
- Hyperparathyroidism 3 0 trials
- Hyperparathyroidism 4 0 trials
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Familial multiple fibrofolliculoma 0 trials
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2 sub-types
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Lung cancer susceptibility 1 0 trials
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Lung cancer susceptibility 3 0 trials
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Lung cancer susceptibility 4 0 trials
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Lung cancer susceptibility 5 0 trials
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3 sub-types
- Mosaic NF2-related schwannomatosis 0 trials
- Mosaic neurofibromatosis type 1 0 trials
- Mosaic schwannomatosis 0 trials
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7 sub-types
- Atelis syndrome 1 0 trials
- Atelis syndrome 2 0 trials
- Mosaic variegated aneuploidy syndrome 1 0 trials
- Mosaic variegated aneuploidy syndrome 2 0 trials
- Mosaic variegated aneuploidy syndrome 3 0 trials
- Mosaic variegated aneuploidy syndrome 4 0 trials
- Mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition 0 trials
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Neuroblastoma, susceptibility to, 1 0 trials
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Neuroblastoma, susceptibility to, 2 0 trials
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Neuroblastoma, susceptibility to, 4 0 trials
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Neuroblastoma, susceptibility to, 5 0 trials
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Neuroblastoma, susceptibility to, 6 0 trials
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Neuroblastoma, susceptibility to, 7 0 trials
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Ovarian cancer, susceptibility to, 1 0 trials
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Susceptibility to uveal melanoma 0 trials
2 sub-types
- Melanoma, uveal, susceptibility to, 1 0 trials
- Melanoma, uveal, susceptibility to, 2 0 trials
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Tumor predisposition syndrome 2 0 trials
Most studied deeper sub-types
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Can an app keep young people with cancer genes on track?
Disease control OngoingThis study tests a software platform called Nest that helps young adults (ages 18-49) with inherited cancer risks manage their care. Participants will use the tool to track screening and share information with doctors and family. Researchers will compare users to non-users to see…
Sponsor: Nest Genomics • Aim: Disease control
Last updated Jul 18, 2026 00:00 UTC
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Digital assistant aims to close gaps in hereditary cancer care
Disease control By invitation onlyThis trial tests a digital tool that helps doctors and patients manage cancer risks linked to hereditary syndromes like BRCA-related breast/ovarian cancer and Lynch syndrome. The tool provides personalized recommendations during primary care visits. Researchers compare care gaps,…
Sponsor: HealthPartners Institute • Aim: Disease control
Last updated Jul 12, 2026 00:00 UTC
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New program aims to close cancer screening gaps for rural families
Disease control By invitation onlyThis study tests a two-year follow-up program for 200 adults with hereditary cancer syndromes like BRCA or Lynch syndrome. Participants get personalized care plans and regular check-ins with a genetics doctor to help them follow cancer prevention and screening guidelines. The goa…
Sponsor: University of Vermont Medical Center • Aim: Disease control
Last updated Jun 27, 2026 09:01 UTC
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Blood test could spot hidden cancers in High-Risk patients
Diagnosis OngoingThis study is developing a blood test to find early-stage tumors in people with hereditary cancer syndromes (high genetic risk for cancer). Researchers will collect blood samples and medical data from about 1,400 participants across Canada. They will also interview patients and d…
Sponsor: University Health Network, Toronto • Aim: Diagnosis
Last updated Jun 27, 2026 08:12 UTC
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Scientists track families to uncover Cancer's hidden causes
Knowledge-focused OngoingThis study looks at people and families who have a high risk of cancer to learn what genes and environmental factors might increase that risk. Over 5,000 participants are followed over time with questionnaires, medical records, and optional genetic testing. No treatment is given,…
Sponsor: National Cancer Institute (NCI) • Aim: Knowledge-focused
Last updated Sep 18, 2026 00:00 UTC
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50,000 samples to unlock secrets of hereditary tumors
Knowledge-focused CancelledThis study will collect blood and tumor tissue from up to 50,000 adults with hereditary or genetic-linked cancers. Researchers will use these samples to create lab-grown tumor models, like mini-tumors, to study how these cancers work and test new treatments. The goal is to better…
Sponsor: University of California, San Francisco • Aim: Knowledge-focused
Last updated Sep 04, 2026 00:00 UTC
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Video lessons may boost cancer gene knowledge
Knowledge-focused OngoingThis study looks at whether short educational videos can help people with inherited cancer gene mutations learn more about their condition. About 43 adults who carry mutations in genes like BRCA1 or BRCA2 will watch the videos and then take a quiz. The goal is to see if this simp…
Sponsor: M.D. Anderson Cancer Center • Aim: Knowledge-focused
Last updated Aug 16, 2026 00:00 UTC
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Can a chatbot help young people navigate cancer risk?
Knowledge-focused OngoingThis study is testing a chatbot and online portal called AYA-RISE to help adolescents and young adults (ages 12-24) who have genetic conditions that raise their cancer risk. The goal is to see if the tool helps them communicate with family and doctors and make informed decisions …
Sponsor: Dana-Farber Cancer Institute • Aim: Knowledge-focused
Last updated Jul 31, 2026 00:00 UTC
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New web tool aims to spread genetic cancer alerts in families
Knowledge-focused OngoingThis study is creating a web-based program to help people with hereditary cancer mutations share their genetic test results with family members. The goal is to increase awareness among at-risk relatives so they can take steps to prevent cancer. The program is designed for patient…
Sponsor: M.D. Anderson Cancer Center • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:08 UTC
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New national registry aims to improve care for rare genetic polyposis syndromes
Knowledge-focused OngoingThis study is a national registry collecting data from 1500 people with familial adenomatous polyposis (FAP) and related conditions across 28 Italian centers. It aims to better understand how these diseases progress, how they are currently managed, and what factors influence outc…
Sponsor: Fondazione IRCCS Istituto Nazionale dei Tumori, Milano • Aim: Knowledge-focused
Last updated Jun 27, 2026 11:00 UTC
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Can a phone call and online tools save lives? new study aims to boost cancer screening in High-Risk patients
Knowledge-focused By invitation onlyThis study tests two simple, scalable methods to help people with inherited cancer risk follow through on recommended screenings. Researchers will provide online educational resources and personalized phone outreach to 900 participants. The goal is to see if these approaches impr…
Sponsor: University of Washington • Aim: Knowledge-focused
Last updated Jun 27, 2026 09:09 UTC
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Deep dive into DNA: new study hunts for hidden hereditary cancer clues
Knowledge-focused OngoingThis study looks at the complete DNA and RNA of 10 people and their families who are at high risk for hereditary cancer but have no known genetic cause. Researchers will use whole genome sequencing and tumor analysis to discover new genetic changes that may lead to cancer. The go…
Sponsor: University Health Network, Toronto • Aim: Knowledge-focused
Last updated Jun 27, 2026 08:01 UTC
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New study tests tools to help families share cancer genetic results
Knowledge-focused OngoingThe IMPACT Study is testing two online tools—GeneSHARE and LivingLabReport—to help people with inherited cancer gene variants share their results with family members and follow cancer screening guidelines. The study involves 720 adults who have a genetic variant linked to cancers…
Sponsor: Vanderbilt-Ingram Cancer Center • Aim: Knowledge-focused
Last updated Jun 26, 2026 18:58 UTC