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Details
Link-It Detail - Disease - Hypoprothrombinemias
Debug Stats
  • ### Total Build Time: 116 ms 23.635 KB
  • CONCEPT_NAME gt=8 ms Completed: 8 ms rowSize= 398 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 208 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=13 ms Completed: 13 ms rowSize= 1.427 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=26 ms Completed: 26 ms rowSize= 5.443 KB
  • CONCEPT_RELATIONSHIPS gt=54 ms Completed: 54 ms rowSize= 13.211 KB
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 1.589 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=2 ms Completed: 2 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hypoprothrombinemias C0020640
Inherited Factor II deficiency
Definition (1)
absence or reduced levels of prothrombin in the blood.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Hemorrhagic Disorders C0019087
img Coagulation Protein Disorders C0600503
img Blood Coagulation Disorders, Inherited C0852077
Ancestral Roots
RootRoot Plus OneDepthParent
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189394img Hemorrhagic Disorders C0019087
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Coagulation Protein Disorders C0600503
img Hemic and Lymphatic Diseases C0018981img Hematologic Diseases C00189395img Blood Coagulation Disorders, Inherited C0852077
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501234img Blood Coagulation Disorders, Inherited C0852077
Relationships (26)

Relation Types:
diso_​to_​chem : 21
diso_​to_​diso : 3
diso_​to_​phen : 2


Relationships:
none : 4
mapped_​to : 1
may_​prevent : 6
may_​treat : 13
permuted_​term_​of : 1
related_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN13img genetic aspects C0017399
DISO_to_CHEM10img Prothrombin C0033706
DISO_to_CHEM8img Prothrombin C0033706
DISO_to_PHEN8img genetic aspects C0017399
DISO_to_CHEMmay_preventimg 1,4-Naphthalenedione, 2-methyl-3-(3,7,11,15-tetramethyl-2-hexadecenyl)-, (R-(R*,R*-(E)))- C0031862
DISO_to_CHEMmay_treatimg 2-Methyl-1,4-naphthalenedione C0025270
DISO_to_CHEMmay_preventimg 2-methyl-1,4-naphthalenediol C0065932
DISO_to_CHEMmay_treatimg COAGULATION FACTOR IX RECOMBINANT 250 UNT INTRAVENOUS INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION C1621474
DISO_to_CHEMmay_treatimg FACTOR IX,RECOMBINANT C0982152
DISO_to_CHEMmay_treatimg FACTOR IX,RECOMBINANT 500 UNT/VIL INJ C0976852
DISO_to_CHEMmay_treatimg Factor IX 100 UNT/ML Injectable Solution C1591335
DISO_to_CHEMmay_treatimg MENADIOL NA DIPHOSPHATE 10MG/ML INJ C0783750
DISO_to_CHEMmay_treatimg MENADIOL NA DIPHOSPHATE 37.5MG/ML INJ C0783751
DISO_to_CHEMmay_preventimg MENADIOL NA DIPHOSPHATE 5MG TAB C0978388
DISO_to_CHEMmay_preventimg MENADIOL NA DIPHOSPHATE 5MG/ML INJ C0783749
DISO_to_CHEMmay_treatimg MENADIONE 25MG/ML INJ,SUSP C0978390
DISO_to_CHEMmay_treatimg Menadiol sodium phosphate C0127514
DISO_to_CHEMmay_treatimg PHYTONADIONE 10 MG INTRAMUSCULAR INJECTION, EMULSION C0979525
DISO_to_CHEMmay_treatimg PHYTONADIONE 5 MG ORAL TABLET C0689999
DISO_to_CHEMmay_treatimg VITAMIN K2 CAP/TAB C2978154
DISO_to_CHEMmay_preventimg Vitamin K C0042878
DISO_to_CHEMmay_treatimg Vitamin K 1 0.1 MG Oral Tablet C0979524
DISO_to_CHEMmay_preventimg Vitamin K 1 2 MG/ML Includes Injectable Solution & 0.5 ML Prefilled Syringe C2713241
DISO_to_DISOmapped_toimg Acquired factor II deficiency C0392610
DISO_to_DISOrelated_toimg Hereditary factor II deficiency disease C0272317
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanF22147coagulation factor II (thrombin)
img GENERIF, Score=901, Pubmed Id: 15892853, UMLKSK CUI: C0020640
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020640Hypoprothrombinemias0self