Severe congenital neutropenia due to JAGN1 deficiency
ORPHA:423384Autosomal dominant severe congenital neutropenia
ORPHA:486Autosomal recessive severe congenital neutropenia
ORPHA:439849Autosomal recessive severe congenital neutropenia due to CSF3R deficiency
ORPHA:420702Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
ORPHA:420699Congenital enteropathy due to enteropeptidase deficiency
ORPHA:168601Congenital neutropenia-combined immunodeficiency due to MKL1 deficiency
ORPHA:619941Congenital plasminogen activator inhibitor type 1 deficiency
ORPHA:465Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
ORPHA:217467Kostmann syndrome
ORPHA:99749Obesity due to congenital leptin deficiency
ORPHA:66628Severe congenital neutropenia
ORPHA:42738Severe congenital neutropenia due to G6PC3 deficiency
ORPHA:331176Severe congenital neutropenia-developmental delay syndrome due to SRP54 deficiency
ORPHA:675767Severe hemophilia A
ORPHA:169802Severe hemophilia B
ORPHA:169793Severe hereditary thrombophilia due to congenital protein C deficiency
ORPHA:745Severe hereditary thrombophilia due to congenital protein S deficiency
ORPHA:743X-linked severe congenital neutropenia
ORPHA:86788