Disease Browser
Parent Node: Infant, Newborn, Diseases (D007232) Parent Node: Thrombocytopenia (D013921) ..Starting node .. Thrombocytopenia, Neonatal Alloimmune (D054098) Child Nodes:
Sister Nodes: ..Absent radii and thrombocytopenia (C536940) ..Acquired pure megakaryocytic aplasia (C538176) ..Congenital amegakaryocytic thrombocytopenia (C535982) ..Congenital disorder of glycosylation type 1X (C535751) ..DK Phocomelia Syndrome (C565618) ..Dyserythropoietic Anemia with Thrombocytopenia (C564525) ..Evan's syndrome (C536380) ..FORSYTHE-WAKELING SYNDROME (OMIM:613606) ..Gardner Morrisson Abbot syndrome (C535643) ..Giant Platelet Syndrome with Thrombocytopenia (C564237) ..Glycoprotein IA Deficiency (C566000) ..Jacobsen Distal 11q Deletion Syndrome (D054868) 1 ..Kasabach-Merritt Syndrome (D059885) 1 ..Macrothrombocytopenia progressive deafness (C537831) ..Macrothrombocytopenia, Autosomal Dominant, Tubb1-Related (C567747) ..Macrothrombocytopenia, X-Linked (C564526) ..MYH9-Related Disorders (C535507) ..Oculootoradial syndrome (C535544) ..Osteochondrodysplasia, Rhizomelic, with Callosal Agenesis, Thrombocytopenia, Hydrocephalus, and Hypertension (C563478) ..Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia (C565328) ..Spastic Paraplegia And Evans Syndrome (C566652) ..Tetraphocomelia-Thrombocytopenia Syndrome (C564771) ..Thrombasthenia-Thrombocytopenia, Hereditary (C566060) ..Thrombocytopenia 1 (C564052) ..THROMBOCYTOPENIA 2 (OMIM:188000) ..Thrombocytopenia 3 (C567487) ..Thrombocytopenia 4 (C567438) ..Thrombocytopenia absent ulnar syndrome (C536944) ..Thrombocytopenia chromosome breakage (C536519) ..Thrombocytopenia Robin sequence (C536898) ..Thrombocytopenia with Elevated Serum Iga and Renal Disease (C564051) ..Thrombocytopenia, cyclic (C536899) ..Thrombocytopenia, Neonatal Alloimmune (D054098) ..Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis (C564050) ..Thrombocytopenia, X-Linked, Intermittent (C564053) ..THROMBOCYTOPENIA, X-LINKED, WITH OR WITHOUT DYSERYTHROPOIETIC ANEMIA (OMIM:300367) ..Thrombotic Microangiopathies (D057049) 9 Human Disease MESH is developed by UMLS . Further data from MedGen , OMIM , CTD
Term ID: 10997
Name: Thrombocytopenia, Neonatal Alloimmune
Definition: A condition in newborns caused by immunity of the mother to PLATELET ALLOANTIGENS on the fetal platelets. The PLATELETS, coated with maternal ANTIBODIES, are destroyed and removed by the fetal MONONUCLEAR PHAGOCYTE SYSTEM. Affected infants may have INTRACRANIAL HEMORRHAGES.
Alternative IDs:
ParentIDs: MESH:D007232|MESH:D013921
TreeNumbers: C15.378.140.855.850 |C16.614.899
Synonyms: Alloimmune Thrombocytopenia, Neonatal |Alloimmune Thrombocytopenias, Neonatal |Neonatal Alloimmune Thrombocytopenia |Neonatal Alloimmune Thrombocytopenias |Neonatal Thrombocytopenia |Neonatal Thrombocytopenias |Thrombocytopenia, Neonatal |Thrombocytopenias, Neo
Slim Mappings: Blood disease|Infant-newborn disease
Reference:
MedGen: D054098
MeSH: D054098
OMIM: Genes: Phenotypes Disease Causing ClinVar Variants