K63.9
BillableDisease of intestine, unspecified
Disease of intestine, unspecified
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Also Known As / Clinical Terms
SNOMED CT
- Congenital keratoderma6874009
- Megaloblastic anaemia due to impaired absorption of folate27798002
- Megaloblastic anemia due to impaired absorption of folate27798002
- Cathartic colon40857009
- Intestinal autonomic neuropathy45299002
- Alymphocytosis48813009
- Lymphocytopenia48813009
- Lymphopenia48813009
- Megaloblastic anaemia due to disease of small intestine82895008
- Megaloblastic anaemia due to ileal disease82895008
- Megaloblastic anemia due to disease of small intestine82895008
- Megaloblastic anemia due to ileal disease82895008
- Disorder of intestine85919009
- Enteropathy85919009
- Intestinal disease85919009
- CAH - Congenital adrenal hypoplasia93235007
- Congenital adrenal hypoplasia93235007
- Congenital hypoplasia of adrenal gland93235007
- Congenital small adrenal gland93235007
- Disorder of small intestine119522002
- Disorder of large intestine119523007
- Disorder of colon128524007
- Disorder of caecum128525008
- Disorder of cecum128525008
- HIV - Human immunodeficiency virus diarrhea235726002
- HIV - Human immunodeficiency virus diarrhoea235726002
- HIV - Human immunodeficiency virus enteropathy235726002
- Human immunodeficiency virus diarrhea235726002
- Human immunodeficiency virus diarrhoea235726002
- Human immunodeficiency virus enteropathy235726002
- Human immunodeficiency virus non-pathogenic diarrhea235726002
- Human immunodeficiency virus non-pathogenic diarrhoea235726002
- Autoimmune enteropathy235728001
- Gastrointestinal tract problem300439004
- Disorder of jejunum304370001
- Bowel problem309615009
- Disorder of ileum312895004
- Disorder of intestine caused by non-steroidal anti-inflammatory drug700425005
- NSAID (non-steroidal anti-inflammatory drug) induced enteropathy700425005
- Non-steroidal anti-inflammatory drug-induced enteropathy700425005
- Disorder of gastrointestinal tract co-occurrent with human immunodeficiency virus infection713300006
- Megaloblastic anaemia due to vitamin B12 deficiency secondary to intestinal disease717946000
- Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease717946000
- Erythrokeratodermia variabilis 3722035007
- Erythrokeratodermia variabilis Kamouraska type722035007
- Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome722035007
- MEDNIK (mental retardation, enteropathy, deafness, peripheral neuropathy, ichtyosis, keratodermia) syndrome722035007
- MEDNIK syndrome722035007
- Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome722288007
- Lymphocyte count below reference range1156294003
- Autosomal recessive combined immunodeficiency with multiple intestinal atresias1197428008
- CID-MIA/early-onset IBD - combined immunodeficiency-multiple intestinal atresia/early-onset inflammatory bowel disease1197428008
- Combined immunodeficiency due to TTC7A mutation1197428008
- Combined immunodeficiency, enteropathy spectrum1197428008
- MIRAGE (myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy) syndrome1234831009
- MIRAGE syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome1234831009
- Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, enteropathy syndrome1234831009
- Colonic lesion67401000119103
- Short stature co-occurrent and due to endocrine disorder368331000119100
UMLS
- Disease of intestine, unspecifiedC0021831
- Disease, IntestinalC0021831
- Diseases, IntestinalC0021831
- Disorder of intestineC0021831
- Disorder of intestine (disorder)C0021831
- EnteropathyC0021831
- INTESTINAL DISC0021831
- Intestinal DiseaseC0021831
- Intestinal DiseasesC0021831
- Intestinal DisorderC0021831
- Intestinal diseaseC0021831
- Unspecified disorder of intestineC0021831
- bowel diseaseC0021831
- bowel diseasesC0021831
- bowel disorderC0021831
- bowel disordersC0021831
- bowel dysfunctionC0021831
- bowels diseaseC0021831
- bowels diseasesC0021831
- bowels disordersC0021831
- disease bowelC0021831
- disease intestinalC0021831
- disease intestineC0021831
- disease intestinesC0021831
- diseases intestinal tractC0021831
- diseases intestineC0021831
- diseases intestinesC0021831
- diseases of the intestinal tractC0021831
- disorder intestinalC0021831
- disorder intestineC0021831
- disorders bowelC0021831
- disorders intestinalC0021831
- disorders intestineC0021831
- disorders intestinesC0021831
- enteropathyC0021831
- intestinal diseaseC0021831
- intestinal diseasesC0021831
- intestinal disorderC0021831
- intestinal disordersC0021831
- intestinal tract diseasesC0021831
- intestine diseaseC0021831
- intestine disorderC0021831
Frequently Asked Questions
What is the ICD-10 code for disease of intestine, unspecified?
The ICD-10-CM code for disease of intestine, unspecified is K63.9. The full clinical description is "Disease of intestine, unspecified". K63.9 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code K63.9 mean?
ICD-10-CM code K63.9 represents "Disease of intestine, unspecified". It is classified under Chapter 11: Diseases of the Digestive System and is a billable/specific code that can be used on a claim.
Is K63.9 a billable code?
Yes, K63.9 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is K63.9 in?
K63.9 is in Chapter 11: Diseases of the Digestive System (codes K00-K95).
What SNOMED CT codes does K63.9 map to?
K63.9 maps to 28 SNOMED CT concepts: 48813009, 235728001, 722288007, 1197428008, 309615009, and 23 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for K63.9?
K63.9 is linked to 1 UMLS Concept Unique Identifier: C0021831. 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.