acral peeling skin syndrome
autosomal recessive genodermatosis characterized by the shedding of the outer epidermis
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acral peeling skin syndrome
Summary
acral peeling skin syndrome is a rare disease[1].
Key Facts
- acral peeling skin syndrome's instance of is recorded as rare disease[2].
- acral peeling skin syndrome's instance of is recorded as class of disease[3].
- acral peeling skin syndrome's subclass of is recorded as peeling skin syndrome[4].
- acral peeling skin syndrome's MeSH descriptor ID is recorded as C536316[5].
- acral peeling skin syndrome's OMIM ID is recorded as 609796[6].
- acral peeling skin syndrome's Orphanet ID is recorded as 263534[7].
- acral peeling skin syndrome's genetic association is recorded as TGM5[8].
- acral peeling skin syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_263534[9].
- acral peeling skin syndrome's UMLS CUI is recorded as C1853354[10].
- acral peeling skin syndrome's ICD-10-CM is recorded as Q80.8[11].
- acral peeling skin syndrome's GARD rare disease ID is recorded as 12863[12].
- acral peeling skin syndrome's Mondo ID is recorded as MONDO_0012345[13].
- acral peeling skin syndrome's Genetics Home Reference Conditions ID is recorded as acral-peeling-skin-syndrome[14].
- acral peeling skin syndrome's ICD-11 ID is recorded as 1869724137[15].
- acral peeling skin syndrome's UniProt disease ID is recorded as DI-02148[16].