You are using an outdated browser. Please upgrade your browser to improve your experience.

thrombophilia due to protein S deficiency, autosomal recessive

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description A very rare and severe hematologic disorder resulting in thrombosis and secondary hemorrhage usually beginning in early infancy. Some affected individuals develop neonatal purpura fulminans, multifocal thrombosis, or intracranial hemorrhage.
Mondo Term and Equivalent IDs
MONDO:0013791:  thrombophilia due to protein S deficiency, autosomal recessive
UMLS:C3281092: