Z15.09
BillableGenetic susceptibility to other malignant neoplasm
Genetic susceptibility to other malignant neoplasm
Coding Notes
Includes
Conditions included under this code
- confirmed abnormal gene
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- chromosomal anomalies (Q90-Q99)
Code First
The underlying condition must be sequenced before this code
Also Known As / Clinical Terms
SNOMED CT
- Macroencephaly9740002
- Megalencephaly9740002
- Hereditary cancer-predisposing syndrome699346009
- Hereditary neoplastic syndrome699346009
- Mosaic variegated aneuploidy syndrome700056005
- M-CM - macrocephaly capillary malformation700063005
- MCAP - megalencephaly capillary malformation700063005
- Macrocephaly-capillary malformation700063005
- Macrocephaly-cutis marmorata telangiectatica congenita700063005
- Megalencephaly capillary malformation700063005
- Megalencephaly, capillary malformation, polymicrogyria syndrome700063005
- DICER1 syndrome702411003
- Pleuropulmonary blastoma familial tumor and dysplasia syndrome702411003
- Pleuropulmonary blastoma familial tumour and dysplasia syndrome702411003
- Pleuropulmonary blastoma family tumor susceptibility syndrome702411003
- Pleuropulmonary blastoma family tumour susceptibility syndrome702411003
- Lynch syndrome716318002
- Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome722202006
- BAP1 tumor predisposition syndrome765057007
- BAP1 tumour predisposition syndrome765057007
- BAP1-related tumor predisposition syndrome765057007
- BAP1-related tumour predisposition syndrome765057007
- BRCA1 associated protein 1 tumor predisposition syndrome765057007
- BRCA1 associated protein 1 tumour predisposition syndrome765057007
- Tumor susceptibility associated with germline BAP1 mutation765057007
- Tumour susceptibility associated with germline BAP1 mutation765057007
- Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutation766707003
- MITF (melanogenesis associated transcription factor) related melanoma and renal cell carcinoma predisposition syndrome770896003
- MITF-related melanoma and renal cell carcinoma predisposition syndrome770896003
- Melanogenesis associated transcription factor related melanoma and renal cell carcinoma predisposition syndrome770896003
- Familial rhabdoid tumor772130002
- Familial rhabdoid tumour772130002
- Rhabdoid tumor predisposition syndrome772130002
- Rhabdoid tumour predisposition syndrome772130002
- Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome782823001
- DDX41-related haematologic malignancy predisposition syndrome1172625004
- DDX41-related hematologic malignancy predisposition syndrome1172625004
- DEAD-box helicase 41-related haematologic malignancy predisposition syndrome1172625004
- DEAD-box helicase 41-related hematologic malignancy predisposition syndrome1172625004
- Combined immunodeficiency due to CARMIL2 deficiency1186712009
- Combined immunodeficiency due to RLTPR deficiency1186712009
- Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency1186712009
- Combined immunodeficiency due to CD70 deficiency1186715006
- Progeroid features, hepatocellular carcinoma predisposition syndrome1216939003
- Ruijs Aalfs syndrome1216939003
- Hereditary well-differentiated neuroendocrine tumor of small intestine1288023007
- Hereditary well-differentiated neuroendocrine tumour of small intestine1288023007
- Genetic susceptibility to cancer85121000119109
- HNPCC (hereditary non-polyposis colon cancer) gene mutation positive1099611000119109
- Hereditary non-polyposis colon cancer gene mutation detected1099611000119109
- Hereditary non-polyposis colon cancer gene mutation positive1099611000119109
- Hereditary nonpolyposis colon cancer gene mutation positive1099611000119109
Frequently Asked Questions
What is the ICD-10 code for genetic susceptibility to other malignant neoplasm?
The ICD-10-CM code for genetic susceptibility to other malignant neoplasm is Z15.09. The full clinical description is "Genetic susceptibility to other malignant neoplasm". Z15.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Z15.09 mean?
ICD-10-CM code Z15.09 represents "Genetic susceptibility to other malignant neoplasm". It is classified under Chapter 22: Factors Influencing Health Status and Contact With Health Services and is a billable/specific code that can be used on a claim.
Is Z15.09 a billable code?
Yes, Z15.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Z15.09 in?
Z15.09 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).
What codes cannot be used with Z15.09?
Z15.09 has Excludes1 notes indicating codes that cannot be used together with it, including: chromosomal anomalies (Q90-Q99).
Are additional codes required with Z15.09?
Yes, when using Z15.09 you should also code: code, if applicable, for any associated family history of the disease (Z80-Z84); code, if applicable, for any personal history of malignant neoplasm (Z85.-).
What SNOMED CT codes does Z15.09 map to?
Z15.09 maps to 19 SNOMED CT concepts: 765057007, 1186712009, 1186715006, 1172625004, 702411003, and 14 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Z15.09?
Z15.09 is linked to 1 UMLS Concept Unique Identifier: C1455994. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.