Immunodeficiency 98 with autoinflammation, X-linked

Preferred Label : Immunodeficiency 98 with autoinflammation, X-linked;

Symbol : IMD98;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Inflammation, neutropenia, bone marrow failure, and lymphoproliferation caused by tlr8; INFLTR8;

Prefixed ID : #301078;

Détails

Origin ID

301078;

UMLS CUI

C5676883;

Genes related to phenotype
- Toll-like receptor 8 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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