Q82.0
BillableHereditary lymphedema
Hereditary lymphedema
Status
Billable / Specific
Parent Code
Q82Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Excludes 2
Conditions not included here, but the patient may have both
- inborn errors of metabolism (E70-E88)
Also Known As / Clinical Terms
SNOMED CT
- Distichiasis-lymphedema syndrome8634009
- Distichiasis-lymphoedema syndrome8634009
- Accessory eyelid24606006
- Yellow nails45342007
- Distichiasis95339000
- Reduplication of lashes95339000
- Ectopic cilia of eyelid95504004
- Edema of foot102576009
- Foot edema102576009
- Foot oedema102576009
- Oedema of foot102576009
- Pedal edema102576009
- Pedal oedema102576009
- Atresia of posterior nares204508009
- Atresia of posterior naris204508009
- Choanal atresia204508009
- Congenital atresia of choana204508009
- Congenital atresia of posterior nares204508009
- Amniotic bands of upper limb205299003
- Constriction ring syndrome of upper limb205299003
- Constriction ring syndrome of lower limb205382001
- Constriction ring of lower limb with lymphedema205385004
- Constriction ring of lower limb with lymphoedema205385004
- Congenital elephantiasis205545009
- AVM - Cerebral arteriovenous malformation234142008
- Cerebral arteriovenous malformation234142008
- Congenital cerebral arteriovenous malformation234142008
- Megakaryocytic thrombocytopenia234483004
- Congenital distichiasis253214000
- Hereditary lymphedema254199006
- Hereditary lymphoedema254199006
- Constriction ring of upper limb with lymphedema268264007
- Constriction ring of upper limb with lymphoedema268264007
- Hereditary disorder of lymphatic system363190001
- Hereditary lymphedema type I399889006
- Hereditary lymphoedema type I399889006
- Milroy lymphedema399889006
- Milroy lymphoedema399889006
- Nonne-Milroy lymphedema399889006
- Nonne-Milroy lymphoedema399889006
- Hereditary lymphedema type II400040008
- Hereditary lymphoedema type II400040008
- Meige disease400040008
- Meige lymphedema400040008
- Meige lymphoedema400040008
- Adult lymphedema400158000
- Adult lymphoedema400158000
- Lymphedema tarda400158000
- Lymphedema tardum400158000
- Lymphoedema tarda400158000
- Lymphoedema tardum400158000
- Primary adult lymphedema400158000
- Primary adult lymphoedema400158000
- Primary lymphedema tardum400158000
- Primary lymphoedema tardum400158000
- Hereditary lymphedema and yellow nails400211001
- Hereditary lymphoedema and yellow nails400211001
- Yellow nail syndrome400211001
- Congenital anomaly of cutaneous lymphatics402809007
- Congenital malformation of cutaneous lymphatics402809007
- Congenital malformation of lymphatic vessel of skin402809007
- Lymphedema of leg403385000
- Lymphedema of lower extremity403385000
- Lymphoedema of leg403385000
- Lymphoedema of lower extremity403385000
- Constricting band of extremity403556005
- Lymphedema of upper limb449620005
- Lymphoedema of upper limb449620005
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome720986005
- Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema syndrome720986005
- OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema) syndrome720986005
- OL-EDA-ID (anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphoedema) syndrome720986005
- Lymphedema and cerebral arteriovenous anomaly syndrome721979005
- Lymphoedema and cerebral arteriovenous anomaly syndrome721979005
- HLTRS (hypotrichosis, lymphedema, telangiectasia, renal defect) syndrome723363009
- HLTRS (hypotrichosis, lymphoedema, telangiectasia, renal defect) syndrome723363009
- Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome723363009
- Hypotrichosis, lymphoedema, telangiectasia, renal defect syndrome723363009
- MLCRD (microcephaly with or without chorioretinopathy, lymphedema or intellectual disability) syndrome733604003
- MLCRD (microcephaly with or without chorioretinopathy, lymphoedema or intellectual disability) syndrome733604003
- Microcephalus, lymphedema, chorioretinopathy syndrome733604003
- Microcephalus, lymphoedema, chorioretinopathy syndrome733604003
- Amniotic band syndrome765206003
- Congenital constriction band765206003
- Constriction ring syndrome765206003
- Deformity due to amniotic band765206003
- PEHO-like syndrome770678005
- PEHOL (progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like) syndrome770678005
- PEHOL (progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like) syndrome770678005
- Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome770678005
- Progressive encephalopathy with oedema, hypsarrhythmia, and optic atrophy-like syndrome770678005
- Congenital lymphangiectases788292004
- Congenital lymphangiectasia788292004
- Congenital lymphangiectasis788292004
- Congenital cutaneous lymphangiectasia788294003
- Congenital lymphangiectasia with chylous reflux788295002
- Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Macrothrombocytopenia, lymphoedema, developmental delay, facial dysmorphism, camptodactyly syndrome1172685001
- Takenouchi Kosaki syndrome1172685001
- Disseminated warts, impaired cell-mediated immunity, primary lymphedema, anogenital dysplasia syndrome1186725001
- Disseminated warts, impaired cell-mediated immunity, primary lymphoedema, anogenital dysplasia syndrome1186725001
- WILD (warts, immunodeficiency, lymphedema, anogenital dysplasia) syndrome1186725001
- WILD (warts, immunodeficiency, lymphoedema, anogenital dysplasia) syndrome1186725001
- WILD syndrome1186725001
- Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome1186725001
- Warts, immunodeficiency, lymphoedema, anogenital dysplasia syndrome1186725001
- Lymphedema, posterior choanal atresia syndrome1204421005
- Lymphoedema, posterior choanal atresia syndrome1204421005
- EPHB4-related generalised lymphatic dysplasia with atrial septal defect1222666002
- EPHB4-related generalised lymphatic dysplasia with non-immune hydrops fetalis1222666002
- EPHB4-related generalized lymphatic dysplasia with atrial septal defect1222666002
- EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis1222666002
- EPHB4-related lymphatic-related hydrops fetalis1222666002
- Ephrin receptor B4-related lymphatic-related hydrops fetalis1222666002
- Generalised lymphatic dysplasia of Fotiou1222667006
- Generalized lymphatic dysplasia of Fotiou1222667006
- PIEZO1-related generalised lymphatic dysplasia with non-immune hydrops fetalis1222667006
- PIEZO1-related generalised lymphatic dysplasia with systemic involvement1222667006
- PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis1222667006
- PIEZO1-related generalized lymphatic dysplasia with systemic involvement1222667006
- PIEZO1-related lymphatic-related hydrops fetalis1222667006
- Piezo type mechanosensitive ion channel component 1-related generalised lymphatic dysplasia with non-immune hydrops fetalis1222667006
- Piezo type mechanosensitive ion channel component 1-related generalized lymphatic dysplasia with non-immune hydrops fetalis1222667006
- CELSR1-related late-onset primary lymphedema1222668001
- CELSR1-related late-onset primary lymphoedema1222668001
- Cadherin EGF LAG seven-pass G-type receptor 1-related late-onset primary lymphedema1222668001
- Cadherin EGF LAG seven-pass G-type receptor 1-related late-onset primary lymphoedema1222668001
- Congenital primary lymphedema of Gordon1222669009
- Congenital primary lymphoedema of Gordon1222669009
- VEGFC-related congenital primary lymphedema1222669009
- VEGFC-related congenital primary lymphoedema1222669009
- GJC2-related late-onset primary lymphedema1222670005
- GJC2-related late-onset primary lymphoedema1222670005
- Gap junction protein gamma 2-related late-onset primary lymphedema1222670005
- Gap junction protein gamma 2-related late-onset primary lymphoedema1222670005
Frequently Asked Questions
What is ICD-10 code Q82.0?
ICD-10-CM code Q82.0 represents "Hereditary lymphedema". It is a billable/specific code that can be used on a claim.
Is Q82.0 a billable code?
Yes, Q82.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is Q82.0 in?
Q82.0 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).
What codes cannot be used with Q82.0?
Q82.0 has Excludes1 notes indicating codes that cannot be used together with it, including: acrodermatitis enteropathica (E83.2); congenital erythropoietic porphyria (E80.0); pilonidal cyst or sinus (L05.-); and 1 more.
What SNOMED CT codes does Q82.0 map to?
Q82.0 maps to 42 SNOMED CT concepts: 234142008, 24606006, 400158000, 765206003, 205299003, and 37 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for Q82.0?
Q82.0 is linked to 1 UMLS Concept Unique Identifier: C5779780. 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.