| ICD Code |
Disorder |
E78.660:
|
Tangier disease |
E78.810:
|
Hyalinosis cutis et mucosae |
E78.810:
|
Lipoid proteinosis |
E78.810:
|
Lipoid proteinosis |
E78.810:
|
Urbach Wiethe disease |
E78.820:
|
Hyalinosis, systemic |
E78.830:
|
Multicentric reticulohistiocytosis |
E78.830:
|
Multicentric reticulohistiocytosis |
E79.100:
|
Lesch-Nyhan syndrome |
E80.010:
|
Erythropoietic protoporphyria |
E80.010:
|
Protoporphyria erythropoeitic |
E80.020:
|
Erythropoietic porphyria, congenital |
E80.020:
|
Gunther's disease |
E80.030:
|
Porphyria, erythropoietic |
E80.040:
|
Erythropoietic coproporphyria |
E80.100:
|
Porphyria cutanea tarda |
E80.110:
|
Porphyria cutanea tarda, sporadic |
E80.120:
|
Porphyria cutanea tarda, familial |
E80.200:
|
Porphyrin abnormality affecting the skin (NEC/NOS) |
E80.210:
|
Acute intermittent porphyria |
E80.210:
|
Porphyria, acute intermittent |
E80.220:
|
Coproporphyria, hereditary |
E80.222:
|
Hereditary coproporphyria |
E80.230:
|
Variegate porphyria |
E80.232:
|
Chester porphyria |
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