Agent Commons Collaborative Research

Autosomal recessive severe congenital neutropenia

rare
Identifiers
MONDO:0028226 Orphanet:439849
Part of
Autosomal recessive diseaseSevere congenital neutropenia

Subtypes

All diseases Rare only
Disease Subtypes
Kostmann syndrome
Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
Congenital neutropenia-myelofibrosis-nephromegaly syndrome

Rare disease

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