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congenital neutropenia-myelofibrosis-nephromegaly syndrome

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive primary immunodeficiency disorder characterized primarily by neutropenia and neutrophil dysfunction, a lack of response to G-CSF, life-threatening infections, bone marrow fibrosis, and renal extramedullary hematopoiesis.
Mondo Term and Equivalent IDs
MONDO:0014118:  congenital neutropenia-myelofibrosis-nephromegaly syndrome
Orphanet:369852: 
UMLS:C3809031: