Kasabach-Merritt syndrome (KMS), also known as hemangioma-thrombocytopenia syndrome, is a rare disorder characterized by profound thrombocytopenia, microangiopathic hemolytic anemia, and subsequent consumptive coagulopathy in association with vascular tumors, particularly kaposiform hemangioendothelioma or tufted angioma. [ Orphanet:2330 ]
Synonyms: hemangiomatosis with thrombocytopenia Kasabach Merritt syndrome Kasabach-Merritt Phenomenon thrombocytopenia-hemangioma syndrome Kasabach Merritt phenomenon hemangioma-thrombocytopenia syndrome hemangioma-hemorrhage syndrome Kasabach-Merritt syndrome thrombopenia-hemangioma syndrome
Term information
- NORD:1320 (MONDO:NORD)
- SCTID:86635005 (MONDO:equivalentTo)
- MESH:D059885 (MONDO:equivalentTo)
- Orphanet:2330 (OMIM:141000)
- NANDO:2100297 (https://orcid.org/0000-0003-0011-764X)
- GARD:70 (MONDO:GARD)
- NANDO:2201035 (https://orcid.org/0000-0003-0011-764X)
- UMLS:C0221025 (MONDO:equivalentTo)
- NCIT:C3821 (MONDO:equivalentTo)
- ICD9:287.39 (MONDO:relatedTo)
- MedDRA:10058423 (Orphanet:2330/e)
- MEDGEN:65122 (MONDO:equivalentTo)
- OMIM:141000 (Orphanet:2330/e)
gard_rare, ordo_disorder, rare, ordo_clinical_situation, nord_rare, orphanet_rare
http://identifiers.org/medgen/65122
http://linkedlifedata.com/resource/umls/id/C0221025
https://omim.org/entry/141000
http://purl.obolibrary.org/obo/NCIT_C3821
http://identifiers.org/mesh/D059885
http://identifiers.org/snomedct/86635005
http://www.orpha.net/ORDO/Orphanet_2330