hypoprothrombinemia

Summary

hypoprothrombinemia is a rare disease^[1]. hypoprothrombinemia is known by 6 alternative names across languages and contexts.^[2]

Key Facts

• hypoprothrombinemia's instance of is recorded as rare disease^[3].
• hypoprothrombinemia's instance of is recorded as class of disease^[4].
• hypoprothrombinemia is a type of autosomal recessive disease^[5].
• hypoprothrombinemia is a type of blood coagulation disease^[6].
• hypoprothrombinemia is a type of congenital vitamin K-dependent coagulation factors deficiency^[7].
• hypoprothrombinemia is a type of reduced prothrombin activity^[8].
• hypoprothrombinemia is a type of thrombophilia^[9].
• hypoprothrombinemia's symptoms and signs is recorded as bleeding^[10].
• hypoprothrombinemia's ICD-9-CM is recorded as 286.3^[11].
• hypoprothrombinemia's NCI Thesaurus ID is recorded as C26799^[12].
• hypoprothrombinemia's NCI Thesaurus ID is recorded as C131737^[13].
• hypoprothrombinemia's health specialty is recorded as hematology^[14].
• hypoprothrombinemia's drug or therapy used for treatment is recorded as menadione^[15].
• hypoprothrombinemia's drug or therapy used for treatment is recorded as menadiol^[16].
• hypoprothrombinemia's genetic association is recorded as F2^[17].
• hypoprothrombinemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2235^[18].
• hypoprothrombinemia's exact match is recorded as http://identifiers.org/doid/DOID:2235^[19].
• hypoprothrombinemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_325^[20].
• hypoprothrombinemia's on focus list of Wikimedia project is recorded as WikiProject Medicine^[21].

Why It Matters

hypoprothrombinemia is known by 6 alternative names across languages and contexts.^[2]