Z83.49
BillableFamily history of endo, nutritional and metabolic diseases
Family history of other endocrine, nutritional and metabolic diseases
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
Code Also
A second code may be required; sequencing depends on circumstances
Related Codes(3)
Also Known As / Clinical Terms(194)
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
UMLS
Clinical Terms
- Family history of lysosomal storage disease
- Family history of combined hyperlipidemia
- Family history of glycogen storage disease
- Family history of endocrine disorders
- Family history of hyperlipidemia
- Family history of neuropathy
- Maternal nutritional disorder
- Family history of hyperbetalipoproteinemia
- Family history of tuberous xanthoma
- Family history of hypercholesterolaemia in first degree relative
- Family history: Hypercholesterolemia
- Family history: Triglyceride high
- FH: Fats raised
- Family history of hyperlipidaemia
- Family history of haemochromatosis
- Family history of combined hyperlipidaemia
- Family history of methylmalonic acidemia
- FH: Hypercholesterolemia
- Family history of cobalamin deficiency
- FH: Endocrine disorders
- Family history of WD-Wilson disease
- Family history of hyperbetalipoproteinaemia
- Family history of hypoalphalipoproteinemia
- FH: Cystic fibrosis
- Family history of vitamin B12 deficiency
- Family history: Metabolic disorder
- Family history: Raised blood lipids
- Family history of hemochromatosis
- Family history of galactosemia
- Family history of 5,10 methylenetetrahydrofolate reductase deficiency
- FH: Obesity
- Family history of Canavan disease
- Family history of hyperthyroidism
- Family history of Addison disease
- FH: Thyroid disorder
- Family history of Graves disease
- Family history of butyrylcholinesterase deficiency
- Family history of mitochondrial disease
- Family history of lung disease
- Family history of Tay-Sachs disease
- FH: Metabolic disorder
- Family history: Obesity
- Family history of eruptive xanthoma
- Family history: Cystic fibrosis
- Family history of hyperparathyroidism
- Family history: Gout
- Family history: Porphyria
- FH: Raised blood lipids
- Family history of galactosaemia
- Family history of acetylcholinesterase deficiency
- Family history: Hypercholesterolaemia in first degree relative
- FH: Haemochromatosis
- Family history of Graves' disease
- Family history of liver disorder
- FH: Thyroid disease
- Family history of polycystic ovary
- Family history of hypoalphalipoproteinaemia
- FH: Hypercholesterolaemia in first degree relative
- Family history of vitamin D deficiency
- FH: Liver disease
- FH: Triglyceride high
- Family history of disorder of lung
- Family history of spongy degeneration of central nervous system
- Family history of polycystic ovaries
- FH: Hypercholesterolemia in first degree relative
- FH: Hypercholesterolaemia
- Family history: Endocrine disorders
- Family history of endocrine disease
- Family history of cystic fibrosis
- Family history of nutritional disorder
- Family history of hypertriglyceridaemia
- Family history of methylmalonic aciduria
- Family history: Hypercholesterolemia in first degree relative
- Family history: Thyroid disorder
- Family history of pseudocholinesterase deficiency
- Family history: Hypothyroidism
- Family history of Hashimoto thyroiditis
- FH: Nutritional deficiency
- Family history of hypercholesterolemia in first degree relative
- Family history of Wilson disease
- FH: Porphyria
- Family history: Nutritional deficiency
- Family history: Liver disease
- Family history of hypertriglyceridemia
- Family history: Hypercholesterolaemia
- FH: Hypothyroidism
- Family history of Addison's disease
- Family history of impaired glucose tolerance
- Family history of metabolic disorder
- Family history of movement disorder
- Family history of phenylketonuria
- FH: Fibrocystic disease
- Family history of tall stature
- Family history: Haemochromatosis
- FH: Gout
- Family history of alpha-1-antitrypsin deficiency
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.
How does Z83.49 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like family history of endo, nutritional and metabolic diseases 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 Z83.49?
There is no direct ICD-11 mapping available for Z83.49 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.