Erythrokeratodermia
human disease
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Erythrokeratodermia
Summary
Erythrokeratodermia is a hereditary disorder[1].
Key Facts
- Erythrokeratodermia's instance of is recorded as hereditary disorder[2].
- Erythrokeratodermia's instance of is recorded as class of disease[3].
- Erythrokeratodermia's subclass of is recorded as erythroderma[4].
- Erythrokeratodermia's subclass of is recorded as epidermal disease[5].
- Erythrokeratodermia's Orphanet ID is recorded as 79355[6].
- Erythrokeratodermia's ICD-9-CM is recorded as 757.39[7].
- Erythrokeratodermia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79355[8].
- Erythrokeratodermia's UMLS CUI is recorded as C0432330[9].
- Erythrokeratodermia's Mondo ID is recorded as MONDO_0019270[10].
- Erythrokeratodermia's Microsoft Academic ID is recorded as 2780580055[11].