Autoinflammatory syndrome, familial, X-linked, behcet-like 2

Preferred Label : Autoinflammatory syndrome, familial, X-linked, behcet-like 2;

Symbol : AIFBL2;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Deficiency in elf4, X-linked; DEX;

Prefixed ID : #301074;

Détails

Origin ID

301074;

UMLS CUI

C5575495;

Genes related to phenotype
- E74-like ets transcription factor 4 [OMIM gene]
ORDO concept(s)
- Hereditary pediatric Behçet-like disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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