BIOMAT Database Logo BIOMAT Database Logo

[Isolated familial factor X deficiency. (Demonstration of recessive hereditary factors)]. 1969

R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl

UI MeSH Term Description Entries
D007020 Hypoprothrombinemias Absence or reduced levels of PROTHROMBIN in the blood. Factor II Deficiency,Prothrombin Deficiency,Deficiency, Factor II,Hypoprothrombinemia,Deficiencies, Factor II,Deficiencies, Prothrombin,Deficiency, Prothrombin,Factor II Deficiencies,Prothrombin Deficiencies
D008297 Male Males
D001779 Blood Coagulation Factors Endogenous substances, usually proteins, that are involved in the blood coagulation process. Clotting Factor,Coagulation Factors,Blood Coagulation Factor,Clotting Factors,Coagulation Factor,Coagulation Factor, Blood,Coagulation Factors, Blood,Factor, Coagulation,Factors, Coagulation,Factor, Blood Coagulation,Factor, Clotting,Factors, Blood Coagulation,Factors, Clotting
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D002869 Chromosome Aberrations Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS. Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality
D003241 Consanguinity The magnitude of INBREEDING in humans. Inbreeding, Human,Consanguineous Marriage,Consanguinous Mating,Consanguineous Marriages,Consanguinities,Consanguinous Matings,Human Inbreeding,Human Inbreedings,Inbreedings, Human,Marriage, Consanguineous,Marriages, Consanguineous,Mating, Consanguinous,Matings, Consanguinous
D005170 Factor X Storage-stable glycoprotein blood coagulation factor that can be activated to factor Xa by both the intrinsic and extrinsic pathways. A deficiency of factor X, sometimes called Stuart-Prower factor deficiency, may lead to a systemic coagulation disorder. Autoprothrombin III,Coagulation Factor X,Stuart Factor,Stuart-Prower Factor,Blood Coagulation Factor X,Factor 10,Factor Ten,Stuart Prower Factor,Factor X, Coagulation
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000293 Adolescent A person 13 to 18 years of age. Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths

Related Publications

R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
[Familial deficiency of factor X].
June 1958, Klinische Wochenschrift,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
[Familial deficiency of factor X].
January 1973, Sangre,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
Hereditary coagulation factor X deficiency.
December 2005, Indian pediatrics,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
Hereditary Factor X (Stuart-Prower Factor) Deficiency.
July 2008, Medical journal, Armed Forces India,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
[Isolated deficiency of growth hormone. 2 brothers with hereditary autosomic recessive genes].
November 1977, Revista clinica espanola,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
[Clinical studies of familial hereditary factor VII deficiency (author's transl)].
May 1981, Blut,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
[Familial hemorrhagic diathesis caused by factor X deficiency].
October 1979, Polski tygodnik lekarski (Warsaw, Poland : 1960),
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiency.
January 2000, American journal of medical genetics,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
[Hereditary factors in congenital deficiency of factor VII].
October 1958, Helvetica medica acta,
R Kurz, and J Glatzl, and F Holzknecht, and F Spöttl
X-linked recessive familial exudative vitreoretinopathy.
August 1992, American journal of ophthalmology,
Copied contents to your clipboard!