Diagnosis Code

Q82.0 HEREDITARY LYMPHEDEMA


Code Information

Diagnosis Code: Q82.0

Short Description: Hereditary lymphedema

Long Description: Hereditary lymphedema

The code Q82.0 is VALID for claim submission

Code Classification:

  • Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • Other congenital malformations (Q80-Q89)
      • Other congenital malformations of skin (Q82)
        • Q82.0 Hereditary lymphedema

Code Version: 2022 ICD-10-CM


Synonyms

  • Accessory eyelid
  • Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome
  • CELSR1-related late-onset primary lymphedema
  • Cerebral arteriovenous malformation
  • Choanal atresia
  • Congenital atresia of nares
  • Congenital atresia of nasopharynx
  • Congenital atresia of pharynx
  • Congenital cutaneous lymphangiectasia
  • Congenital distichiasis
  • Congenital elephantiasis
  • Congenital lymphangiectasia
  • Congenital lymphangiectasia with chylous reflux
  • Congenital malformation of lymphatic vessel of skin
  • Congenital primary lymphedema of Gordon
  • Constricting band of extremity
  • Constricting band of extremity
  • Constriction ring of lower limb with lymphedema
  • Constriction ring of upper limb with lymphedema
  • Constriction ring syndrome
  • Constriction ring syndrome
  • Constriction ring syndrome of lower limb
  • Constriction ring syndrome of upper limb
  • Distichiasis
  • Distichiasis-lymphedema syndrome
  • Ectopic cilia of eyelid
  • Edema of foot
  • EPHB4-related lymphatic-related hydrops fetalis
  • GJC2-related late-onset primary lymphedema
  • Hereditary disorder of lymphatic system
  • Hereditary lymphedema
  • Hereditary lymphedema and yellow nails
  • Hereditary lymphedema type I
  • Hereditary lymphedema type II
  • Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
  • Lymphedema and cerebral arteriovenous anomaly syndrome
  • Lymphedema of lower extremity
  • Lymphedema of lower extremity
  • Lymphedema of lower extremity
  • Lymphedema of upper limb
  • Lymphedema, posterior choanal atresia syndrome
  • Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome
  • Megakaryocytic thrombocytopenia
  • Microcephalus, lymphedema, chorioretinopathy syndrome
  • PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis
  • Primary lymphedema tardum
  • Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome
  • Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome
  • Yellow nails

Diagnostic Related Group(s)

The code Q82.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)
  • Minor Skin Disorders With Mcc (606)
  • Minor Skin Disorders Without Mcc (607)

Crosswalk Information

ICD-10 Code ICD-9 Code ICD-9 Description
Q82.0 Right Arrow 757.0 Hereditary edema of legs

This ICD-10 to ICD-9 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-10 Code ICD-10 Description
Q82 Other congenital malformations of skin
Q82.1 Xeroderma pigmentosum
Q82.2 Congenital cutaneous mastocytosis
Q82.3 Incontinentia pigmenti
Q82.4 Ectodermal dysplasia (anhidrotic)
Q82.5 Congenital non-neoplastic nevus
Q82.6 Congenital sacral dimple
Q82.8 Other specified congenital malformations of skin
Q82.9 Congenital malformation of skin, unspecified


This page was last updated on: 10/1/2023