Z83.49
BillableFamily history of endo, nutritional and metabolic diseases
Family history of other endocrine, nutritional and metabolic diseases
Coding Notes
Also Known As / Clinical Terms
SNOMED CT
- FH: Endocrine disorders160301004
- Family history of endocrine disease160301004
- Family history of endocrine disorders160301004
- Family history: Endocrine disorders160301004
- FH: Thyroid disease160302006
- FH: Thyroid disorder160302006
- Family history: Thyroid disorder160302006
- FH: Metabolic disorder160305008
- Family history of metabolic disorder160305008
- Family history: Metabolic disorder160305008
- FH: Nutritional deficiency160306009
- Family history: Nutritional deficiency160306009
- FH: Gout160308005
- Family history: Gout160308005
- FH: Cystic fibrosis160309002
- FH: Fibrocystic disease160309002
- Family history of cystic fibrosis160309002
- Family history: Cystic fibrosis160309002
- FH: Porphyria160310007
- Family history: Porphyria160310007
- FH: Obesity160311006
- Family history: Obesity160311006
- FH: Hypercholesterolaemia160314003
- FH: Hypercholesterolemia160314003
- Family history: Hypercholesterolaemia160314003
- Family history: Hypercholesterolemia160314003
- FH: Fats raised266887003
- FH: Raised blood lipids266887003
- Family history: Raised blood lipids266887003
- FH: Liver disease266902008
- Family history of liver disorder266902008
- Family history: Liver disease266902008
- FH: Triglyceride high275939003
- Family history of hypertriglyceridaemia275939003
- Family history of hypertriglyceridemia275939003
- Family history: Triglyceride high275939003
- Maternal nutritional disorder288254005
- FH: Hypothyroidism300934004
- Family history: Hypothyroidism300934004
- FH: Haemochromatosis401119001
- Family history of haemochromatosis401119001
- Family history of hemochromatosis401119001
- Family history: Haemochromatosis401119001
- Family history of polycystic ovaries412783008
- Family history of polycystic ovary412783008
- FH: Hypercholesterolaemia in first degree relative417072001
- FH: Hypercholesterolemia in first degree relative417072001
- Family history of hypercholesterolaemia in first degree relative417072001
- Family history of hypercholesterolemia in first degree relative417072001
- Family history: Hypercholesterolaemia in first degree relative417072001
- Family history: Hypercholesterolemia in first degree relative417072001
- Family history of impaired glucose tolerance429971003
- Family history of hyperthyroidism430089002
- Family history of disorder of lung430564002
- Family history of lung disease430564002
- Family history of movement disorder430809001
- Family history of neuropathy430814002
- Family history of alpha-1-antitrypsin deficiency431912005
- Family history of mitochondrial disease473070008
- Family history of Addison disease699057005
- Family history of Addison's disease699057005
- Family history of hyperlipidaemia725117008
- Family history of hyperlipidemia725117008
- Family history of nutritional disorder737366005
- Family history of acetylcholinesterase deficiency789240000
- Family history of 5,10 methylenetetrahydrofolate reductase deficiency29810001000004100
- Family history of Canavan disease98251000119101
- Family history of spongy degeneration of central nervous system98251000119101
- Family history of Graves disease7310001000004107
- Family history of Graves' disease7310001000004107
- Family history of Hashimoto thyroiditis118651000119105
- Family history of Tay-Sachs disease63901000119104
- Family history of WD-Wilson disease456561000124100
- Family history of Wilson disease456561000124100
- Family history of butyrylcholinesterase deficiency98011000119108
- Family history of pseudocholinesterase deficiency98011000119108
- Family history of cobalamin deficiency10780001000004101
- Family history of vitamin B12 deficiency10780001000004101
- Family history of combined hyperlipidaemia64111000119100
- Family history of combined hyperlipidemia64111000119100
- Family history of eruptive xanthoma109241000119103
- Family history of galactosaemia64081000119105
- Family history of galactosemia64081000119105
- Family history of glycogen storage disease64251000119106
- Family history of hyperbetalipoproteinaemia74131000119101
- Family history of hyperbetalipoproteinemia74131000119101
- Family history of hyperparathyroidism14830001000004107
- Family history of hypoalphalipoproteinaemia74171000119103
- Family history of hypoalphalipoproteinemia74171000119103
- Family history of lysosomal storage disease64171000119108
- Family history of methylmalonic acidemia64131000119105
- Family history of methylmalonic aciduria64131000119105
- Family history of phenylketonuria64161000119102
- Family history of tall stature452621000124109
- Family history of tuberous xanthoma109261000119104
- Family history of vitamin D deficiency456511000124103
Frequently Asked Questions
What is the ICD-10 code for family history of endo, nutritional and metabolic diseases?
The ICD-10-CM code for family history of endo, nutritional and metabolic diseases is Z83.49. The full clinical description is "Family history of other endocrine, nutritional and metabolic diseases". Z83.49 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code Z83.49 mean?
ICD-10-CM code Z83.49 represents "Family history of other endocrine, nutritional and metabolic diseases". 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 Z83.49 a billable code?
Yes, Z83.49 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Z83.49 in?
Z83.49 is in Chapter 22: Factors Influencing Health Status and Contact With Health Services (codes Z00-Z99).
What SNOMED CT codes does Z83.49 map to?
Z83.49 maps to 49 SNOMED CT concepts: 160309002, 160301004, 266887003, 160308005, 401119001, and 44 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Z83.49?
Z83.49 is linked to 1 UMLS Concept Unique Identifier: C0478629. 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.