ICD-10 Lookup - Find Medical Diagnosis Codes
ICD-10 Search Results for epidermolysis-bullosa-q81
| ICD-10-CM Code | Description | Category | Valid for Submission |
|---|---|---|---|
| Q81 | Epidermolysis bullosa | Not Valid | |
| Q81.0 | Epidermolysis bullosa simplex Autosomal recessive epidermolysis bullosa simplex; Autosomal recessive epidermolysis bullosa simplex; Autosomal recessive epidermolysis bullosa simplex; Intermediate epidermolysis bullosa simplex with cardiomyopathy; Epidermolysis bullosa simplex with hypodontia; Epidermolysis bullosa simplex herpetiformis; Epidermolysis bullosa simplex with mottled pigmentation; Epidermolysis simplex superficialis; Lethal autosomal recessive epidermolysis bullosa simplex; Epidermolysis bullosa simplex, Ogna type; Autosomal dominant epidermolysis bullosa simplex; Autosomal dominant epidermolysis bullosa simplex; Autosomal dominant epidermolysis bullosa simplex; Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex; Epidermolysis bullosa simplex; Epidermolysis bullosa simplex due to plakophilin deficiency; Epidermolysis bullosa simplex with circinate migratory erythema; Epidermolysis bullosa simplex with pyloric atresia; Basal epidermolysis bullosa simplex; Basal epidermolysis bullosa simplex; Epidermolysis bullosa simplex with muscular dystrophy; KRT14 related epidermolysis bullosa simplex; Suprabasal epidermolysis bullosa simplex; Epidermolysis bullosa simplex due to BP230 deficiency; Epidermolysis bullosa simplex due to exophilin 5 deficiency; Generalized epidermolysis bullosa simplex; Autosomal recessive epidermolysis bullosa simplex; Autosomal recessive epidermolysis bullosa simplex; Autosomal recessive epidermolysis bullosa simplex; Intermediate epidermolysis bullosa simplex with cardiomyopathy; Epidermolysis bullosa simplex with hypodontia; Epidermolysis bullosa simplex herpetiformis; Epidermolysis bullosa simplex with mottled pigmentation; Lethal autosomal recessive epidermolysis bullosa simplex; Epidermolysis bullosa simplex, Ogna type; Autosomal dominant epidermolysis bullosa simplex; Autosomal dominant epidermolysis bullosa simplex; Autosomal dominant epidermolysis bullosa simplex; Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex; Epidermolysis bullosa simplex; Epidermolysis bullosa simplex due to plakophilin deficiency; Epidermolysis bullosa simplex with circinate migratory erythema; Epidermolysis bullosa simplex with pyloric atresia; Basal epidermolysis bullosa simplex; Basal epidermolysis bullosa simplex; Epidermolysis bullosa simplex with muscular dystrophy; KRT14 related epidermolysis bullosa simplex; Suprabasal epidermolysis bullosa simplex; Epidermolysis bullosa simplex due to BP230 deficiency; Epidermolysis bullosa simplex due to exophilin 5 deficiency; Generalized epidermolysis bullosa simplex; | Valid | |
| Q81.1 | Epidermolysis bullosa letalis Generalized junctional epidermolysis bullosa; Junctional epidermolysis bullosa gravis of Herlitz; Generalized junctional epidermolysis bullosa; Junctional epidermolysis bullosa gravis of Herlitz; | Valid | |
| Q81.2 | Epidermolysis bullosa dystrophica Dominant dystrophic epidermolysis bullosa; Autosomal dominant generalized dystrophic epidermolysis bullosa; Progressive recessive dystrophic epidermolysis bullosa; Dystrophic epidermolysis bullosa; Localized dystrophic epidermolysis bullosa; Localized recessive dystrophic epidermolysis bullosa; Generalized dystrophic epidermolysis bullosa; Generalized recessive dystrophic epidermolysis bullosa mitis; Dominant dystrophic epidermolysis bullosa with absence of skin; Generalized recessive non-mutilating dystrophic epidermolysis bullosa; Dystrophic epidermolysis bullosa inverse type; Recessive dystrophic epidermolysis bullosa; Dystrophic epidermolysis bullosa nails only; Severe generalized recessive dystrophic epidermolysis bullosa; Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type; Centripetalis recessive dystrophic epidermolysis bullosa; Acral dystrophic epidermolysis bullosa; Dominant dystrophic epidermolysis bullosa, albopapular type; Dominant dystrophic epidermolysis bullosa; Autosomal dominant generalized dystrophic epidermolysis bullosa; Progressive recessive dystrophic epidermolysis bullosa; Dystrophic epidermolysis bullosa; Localized dystrophic epidermolysis bullosa; Localized recessive dystrophic epidermolysis bullosa; Generalized dystrophic epidermolysis bullosa; Generalized recessive dystrophic epidermolysis bullosa mitis; Dominant dystrophic epidermolysis bullosa with absence of skin; Generalized recessive non-mutilating dystrophic epidermolysis bullosa; Dystrophic epidermolysis bullosa inverse type; Recessive dystrophic epidermolysis bullosa; Dystrophic epidermolysis bullosa nails only; Severe generalized recessive dystrophic epidermolysis bullosa; Recessive dystrophic epidermolysis bullosa non-Hallopeau Siemens type; Centripetalis recessive dystrophic epidermolysis bullosa; Acral dystrophic epidermolysis bullosa; Dominant dystrophic epidermolysis bullosa, albopapular type; | Valid | |
| Q81.8 | Other epidermolysis bullosa Localized non-Herlitz junctional epidermolysis bullosa; Generalized dystrophic epidermolysis bullosa; Localized junctional epidermolysis bullosa; Localized junctional epidermolysis bullosa; Inverse junctional epidermolysis bullosa; Progressive junctional epidermolysis bullosa ; Generalized junctional epidermolysis bullosa; Generalized junctional epidermolysis bullosa; Junctional epidermolysis bullosa mitis; Cicatricial junctional epidermolysis bullosa; Autosomal dominant epidermolysis bullosa simplex; Junctional epidermolysis bullosa; Aplasia cutis congenita in association with epidermolysis bullosa ; Epidermolysis bullosa pruriginosa; Congenital junctional epidermolysis bullosa-pyloric atresia syndrome; Late-onset junctional epidermolysis bullosa; Junctional epidermolysis bullosa non-Herlitz type; Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome; Congenital junctional epidermolysis bullosa; Congenital junctional epidermolysis bullosa; Localized non-Herlitz junctional epidermolysis bullosa; Generalized dystrophic epidermolysis bullosa; Localized junctional epidermolysis bullosa; Localized junctional epidermolysis bullosa; Inverse junctional epidermolysis bullosa; Progressive junctional epidermolysis bullosa ; Generalized junctional epidermolysis bullosa; Generalized junctional epidermolysis bullosa; Junctional epidermolysis bullosa mitis; Cicatricial junctional epidermolysis bullosa; Autosomal dominant epidermolysis bullosa simplex; Junctional epidermolysis bullosa; Aplasia cutis congenita in association with epidermolysis bullosa ; Epidermolysis bullosa pruriginosa; Congenital junctional epidermolysis bullosa-pyloric atresia syndrome; Late-onset junctional epidermolysis bullosa; Junctional epidermolysis bullosa non-Herlitz type; Late-onset localized junctional epidermolysis bullosa, intellectual disability syndrome; Congenital junctional epidermolysis bullosa; Congenital junctional epidermolysis bullosa; | Valid | |
| Q81.9 | Epidermolysis bullosa, unspecified Nail dystrophy due to epidermolysis bullosa; Localized dystrophic epidermolysis bullosa; Epidermolysis bullosa; Pretibial epidermolysis bullosa; Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome; Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome; Nail dystrophy due to epidermolysis bullosa; Localized dystrophic epidermolysis bullosa; Epidermolysis bullosa; Pretibial epidermolysis bullosa; Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome; Nephrotic syndrome, deafness, pretibial epidermolysis bullosa syndrome; | Valid |