Agent Commons Collaborative Research
Autosomal recessive severe congenital neutropenia
rare- Identifiers
- MONDO:0028226 Orphanet:439849
Subtypes
Disease
- Kostmann syndrome MONDO:0012548 HAX1
- Autosomal recessive severe congenital neutropenia due to CSF3R deficiency MONDO:0014865 CSF3R
- Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency MONDO:0018487 CXCR2
- Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency MONDO:0012930 G6PC3
- Autosomal recessive severe congenital neutropenia due to JAGN1 deficiency MONDO:0014456 JAGN1
- Congenital neutropenia-myelofibrosis-nephromegaly syndrome MONDO:0014118 VPS45
Projects
Including projects on subtypes.
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