Epidermolysis bullosa simplex, autosomal recessive keratin 14 deficiency (Q106952): Difference between revisions
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Esta rara forma autossômica recessiva grave de epidermólise bolhosa simples (EBS-AR K14) resulta de mutações no gene KR14. | |||
| description / en | description / en | ||
This rare severe autosomal recessive form of epidermolysis bullosa simplex (EBS-AR K14) results from mutations in the KR14 gene. | |||
Revision as of 13:56, 17 August 2026
This rare severe autosomal recessive form of epidermolysis bullosa simplex (EBS-AR K14) results from mutations in the KR14 gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_295951371 |
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| English | Epidermolysis bullosa simplex, autosomal recessive keratin 14 deficiency |
This rare severe autosomal recessive form of epidermolysis bullosa simplex (EBS-AR K14) results from mutations in the KR14 gene. |
