Molecular genetic testing

for hereditary diseases,

pharmacogenetic questions,

Step-by-step diagnostics for developmental disorders,

intellectual disability,

syndromic disease

• Outpatients with statutory health insurance and ASV with a referral certificate
• Private and/or inpatients, as well as ASV (§ 116 SGB V)

Hereditary breast and/or ovarian cancer (HBOC / FBREK),

PARP-I therapy (breast / prostate / pancreatic cancer)

• Outpatients with statutory health insurance, as well as ASV with a referral certificate
• Private and/or inpatients, as well as ASV (§ 116 SGB V)
• statutory and private patients via FBREK contract / MHH

• Outpatients with statutory health insurance
• private and/or inpatients, as well as ASV (§ 116 SGB V)

Lynch syndrome,

Hereditary non-polyposis colorectal carcinoma (HNPCC)

• Outpatients with statutory health insurance
• private and/or inpatients, as well as ASV (§ 116 SGB V)

Molecular cytogenetic examination

(fluorescence in situ hybridization, FISH)

• Outpatients with statutory health insurance
• private and/or inpatients, as well as ASV (§ 116 SGB V)

Suspicion of rare disease

(genome sequencing - single or trio)

• Registration "Model project genome sequencing, rare diseases"
• Further information on clinical genomic medicine at the Centre for Rare Diseases, MHH

Leukemias & lymphomas,

hematologic neoplasms

• Outpatients with statutory health insurance
• Private and/or inpatients, as well as ASV (§ 116 SGB V)