AutoICD API

C64.9

Billable

Malignant neoplasm of unsp kidney, except renal pelvis

Malignant neoplasm of unspecified kidney, except renal pelvis

Status

Billable / Specific

Block

C64-C68

Parent Code

C64

Coding Notes

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Related Codes(2)
Also Known As / Clinical Terms(287)

SNOMED CT

Clinical Terms

  • Primary clear cell carcinoma of kidney
  • National Wilms Tumor Study Group Stage I
  • Mucinous tubular and spindle cell renal carcinoma
  • GLOW syndrome
  • Clear cell renal cell carcinoma
  • Primary MiT family translocation renal cell carcinoma
  • Metastatic cystic renal cell carcinoma
  • Renal cell carcinoma
  • Metastatic MiT family translocation renal cell carcinoma
  • Renal malignant tumor
  • Primary collecting duct carcinoma of kidney
  • Renal tumor extends into major vein (renal vein or vena cava) macroscopically
  • Renal tumour finding
  • Primary cystic renal cell carcinoma of kidney
  • Primary renal granular cell carcinoma
  • Transitional cell carcinoma of kidney
  • Metastatic chromophobe renal cell carcinoma
  • Papillary renal cell carcinoma
  • Primary translocation renal cell carcinoma
  • Clear cell papillary renal cell carcinoma
  • National Wilms Tumour Study Group Stage III
  • National Wilms Tumor Study Group Stage IV
  • Sarcoma of kidney
  • WAGR (Wilms tumor, aniridia, genitourinary anomalies and mental retardation) syndrome
  • Primary nephroma
  • Metastatic papillary renal cell carcinoma
  • Papillary cystadenocarcinoma of kidney
  • Clear cell carcinoma of kidney
  • Renal tumour invasion into adrenal gland macroscopically
  • Malignant neoplasm of kidney parenchyma
  • Primary transitional cell carcinoma of kidney
  • Renal tumour invades renal vein macroscopically
  • National Wilms Tumor Study Group Stage III
  • Primary Bellini duct carcinoma
  • Renal tumour extends into major vein (renal vein or vena cava) macroscopically
  • Hypernephroma
  • Renal medullary carcinoma
  • Primary hypernephroma
  • Adrenal gland involved by direct invasion of renal tumor
  • Malignant granular cell tumor
  • Primary malignant neoplasm of kidney
  • Renal cell carcinoma of kidney except renal pelvis
  • Renal tumor extends beyond Gerota's fascia macroscopically
  • Wilms tumor
  • Renal tumour extends beyond Gerota's fascia on macroscopic examination
  • Renal tumor extends beyond Gerota's fascia on macroscopic examination
  • Primary papillary cystadenocarcinoma of kidney
  • 11p partial monosomy syndrome
  • Familial leiomyomatosis and renal cell cancer
  • Hereditary primary clear cell renal cell adenocarcinoma
  • Malignant tumour of kidney parenchyma
  • Local recurrence of malignant tumour of kidney
  • Renal tumor invasion into perinephric tissue macroscopically
  • MiT family translocation renal cell carcinoma
  • National Wilms Tumor Study Group Stage V
  • Primary Wilms tumour
  • Chromophobe renal cell carcinoma
  • Renal tumour extends beyond Gerota fascia macroscopically
  • Metastatic collecting duct renal cell carcinoma
  • Primary clear cell sarcoma of kidney
  • Chromosome 11p13 deletion syndrome
  • Malignant tumour of kidney
  • Hereditary primary clear cell renal cell carcinoma
  • Renal tumor invasion into adrenal gland on macroscopic examination
  • Renal tumor invasion into adrenal gland macroscopically
  • Familial leiomyomatosis with renal carcinoma
  • CCSK - clear cell sarcoma of kidney
  • WAGR syndrome
  • National Wilms Tumour Study Group Stage I
  • Wilms tumour
  • Wilm's tumor
  • Primary Wilms tumor
  • Renal tumor extends beyond Gerota fascia macroscopically
  • Primary renal cell carcinoma
  • Hereditary papillary renal cell carcinoma
  • Cystic partially differentiated nephroblastoma of kidney
  • National Wilms Tumour Study Group Stage II
  • HLRCC - hereditary leiomyomatosis and renal cell cancer
  • Renal tumor invades renal vein macroscopically
  • Primary malignant granular cell tumor
  • Renal tumour invasion into adrenal gland on macroscopic examination
  • Bellini carcinoma
  • Cystadenocarcinoma of kidney
  • Deletion of part of chromosome 11
  • Global developmental delay, lung cysts, overgrowth, Wilms tumour syndrome
  • Primary tubulocystic renal cell carcinoma
  • Malignant tumor of kidney
  • Bellini duct carcinoma
  • Malignant cystic nephroma
  • Primary nephroblastoma
  • Collecting duct carcinoma of kidney
  • Cystic renal cell carcinoma of kidney
  • Local recurrence of malignant tumor of kidney
  • Primary sarcoma of retroperitoneum
  • Adrenal gland involved by direct invasion of renal tumour
  • Metastatic translocation renal cell carcinoma
  • Renal tumor grossly extends into major vein (renal vein or vena cava)
  • Primary papillary renal cell carcinoma
  • Hereditary leiomyomatosis and renal cell cancer
  • Renal mucinous tubular and spindle cell carcinoma
  • Metastatic renal cell carcinoma
  • National Wilms Tumor Study Group Stage finding
  • Hereditary leiomyomatosis with renal carcinoma
  • Renal tumor finding
  • Acquired cystic disease associated renal cell carcinoma
  • Familial renal cell carcinoma
  • Cutaneous leiomyoma
  • Renal malignant tumour
  • Renal granular cell carcinoma
  • Leiomyoma cutis
  • Primary malignant granular cell tumour
  • National Wilms Tumor Study Group Stage II
  • National Wilms Tumour Study Group Stage finding
  • WAGR (Wilms tumour, aniridia, genitourinary anomalies and mental retardation) syndrome
  • Primary chromophobe renal cell carcinoma
  • Renal tumour extends beyond Gerota's fascia macroscopically
  • Nephroblastoma
  • Renal cancer
  • Local recurrence of malignant neoplasm of kidney
  • National Wilms Tumour Study Group Stage V
  • Clear cell sarcoma of kidney
  • Primary renal mucinous tubular and spindle cell carcinoma
  • Renal tumour grossly extends into major vein (renal vein or vena cava)
  • Wilms tumour, aniridia, genitourinary anomalies and mental retardation syndrome
  • Primary mucinous tubular and spindle cell renal carcinoma
  • National Wilms Tumour Study Group Stage IV
  • Primary cystadenocarcinoma of kidney
  • Global developmental delay, lung cysts, overgrowth, Wilms tumor syndrome
  • Primary renal medullary carcinoma
  • Renal collecting duct carcinoma
  • Translocation renal cell carcinoma
  • Renal tumour invasion into perinephric tissue macroscopically
  • Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
  • Malignant granular cell tumour
  • Hereditary leiomyomatosis and renal cell carcinoma
  • Tubulocystic renal cell carcinoma
  • GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumor) syndrome
  • Primary renal collecting duct carcinoma
  • GLOW (global developmental delay, lung cysts, overgrowth, Wilms tumour) syndrome
  • Metastatic clear cell renal cell carcinoma
  • Malignant tumor of kidney parenchyma
  • Malignant neoplasm of kidney
Frequently Asked Questions
What is the ICD-10 code for malignant neoplasm of unsp kidney, except renal pelvis?

The ICD-10-CM code for malignant neoplasm of unsp kidney, except renal pelvis is C64.9. The full clinical description is "Malignant neoplasm of unspecified kidney, except renal pelvis". C64.9 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code C64.9 mean?

ICD-10-CM code C64.9 represents “Malignant neoplasm of unspecified kidney, except renal pelvis”. It is classified under Chapter 2: Neoplasms and is a billable/specific code that can be used on a claim.

Is C64.9 a billable code?

Yes, C64.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is C64.9 in?

C64.9 is in Chapter 2: Neoplasms (codes C00-D49).

What codes cannot be used with C64.9?

C64.9 has Excludes1 notes indicating codes that cannot be used together with it, including: malignant carcinoid tumor of the kidney (C7A.093); malignant neoplasm of renal calyces (C65.-); malignant neoplasm of renal pelvis (C65.-).

What SNOMED CT codes does C64.9 map to?

C64.9 maps to 74 SNOMED CT concepts: 4135001, 764856008, 396212001, 733470002, 1187464007, and 69 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for C64.9?

C64.9 is linked to 1 UMLS Concept Unique Identifier: C2845891. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does C64.9 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like malignant neoplasm of unsp kidney, except renal pelvis affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of C64.9?

There is no direct ICD-11 mapping available for C64.9 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.