Hereditary disorder (DBCOND0008301)

Identifiers

Synonyms
Genetic Disorder / Genetic Disorders / Genetic disease (disorder) / Hereditary disease (disorder) / Hereditary Diseases / Hereditary disorder NOS

Associated Data

Indicated Drugs and Targets
DrugDescriptionTargets
Calcium gluconate
An ingredient found in a variety of supplements and vitamins, and is used to lower potassium in the blood or treat magnesium poisoning.
No drug targets
Clinical Trials
IdentifierTitleDrug(s)PurposePhaseStatus
NCT03589079
Delineation of Novel Monogenic Disorders in the United Arab Emirates PopulationNo drug interventionsNot AvailableNot Availableunknown_status
NCT02769949
Pediatric Patients With Metabolic or Other Genetic DisordersNo drug interventionsNot AvailableNot Availablerecruiting
NCT05737602
Promoting Stress Management and Resilience Among Individuals With Von Hippel- Lindau DiseaseNo drug interventionssupportive_careNot Availableenrolling_by_invitation
NCT01851447
Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular DystrophyNo drug interventionsNot AvailableNot Availableactive_not_recruiting
NCT05212428
DNA Sequencing in Clinical Practice, Mayo Clinic Health Tapestry StudyNo drug interventionsscreeningNot Availablerecruiting
NCT00025870
Studies of Children With Metabolic and Other Genetic DisordersNo drug interventionsNot AvailableNot Availablecompleted
NCT01327924
Usability and Tolerability of the Norditropin NordiFlex® Injection Device in Children Never Previously Treated With Growth HormoneNot AvailableNot Availablecompleted
NCT01734486
Growth Response in Girls With Turner Syndrometreatment4completed
NCT00358657
Fludarabine Phosphate, Cyclophosphamide, and Total-Body Irradiation Followed by Donor Bone Marrow Transplant and Cyclophosphamide, Mycophenolate Mofetil, Tacrolimus, and Sirolimus in Treating Patients With Primary Immunodeficiency Disorders or Noncancerous Inherited Disorderstreatment2terminated
NCT04743466
Evaluation of Association Between Testosterone Levels, Dementia, and Adverse Mental Health OutcomesNo drug interventionsNot AvailableNot Availablerecruiting
NCT06362473
Lipid Transport Disorder Italian Genetic Record (LIPIGEN)No drug interventionsNot AvailableNot Availablerecruiting
NCT03435627
Post Marketing Surveillance on Long-term Use With Norditropin® (Short Stature Due to Noonan Syndrome)Not AvailableNot Availablecompleted
NCT01516229
Special Survey for Long Term ApplicationNot AvailableNot Availablecompleted
NCT01435629
A Survey Collecting Data on Adult Height in Patients With Achondroplasia Treated With SomatropinNot AvailableNot Availablecompleted
NCT01529944
Genetic Testing of Noonan Subjects Previously Treated With Norditropin®. An Extension to Trial GHNOO-1658treatment3completed
NCT00705172
Retrospective Observational Study on Efficacy and Safety of Norditropin® in Children With Prader-Willi SyndromeNot AvailableNot Availablecompleted
NCT04681781
SLC13A5 Deficiency Natural History Study - Remote OnlyNo drug interventionsNot AvailableNot Availableenrolling_by_invitation
NCT03065114
Retrospective Study on Clinical Results of Preimplantation Genetic Screening at Different Embryo StageNo drug interventionsNot AvailableNot Availablecompleted
NCT01500447
Inherited Reproductive DisordersNo drug interventionsNot AvailableNot Availablerecruiting
NCT01927861
Investigating the Long-term Efficacy and Safety of Two Doses of NN-220 (Somatropin) in Short Stature Due to Noonan Syndrometreatment3completed
NCT01604161
Non-interventional Study of Patients Using Norditropin® for Growth Hormone Deficiency or Turner SyndromeNot AvailableNot Availablecompleted
NCT00960128
Observational Prospective Study on Patients Treated With Norditropin®Not AvailableNot Availablecompleted
NCT01135537
Pharmacokinetics of Thymoglobulin in Paediatric Haematopoietic Stem-cell Transplantstreatment2terminated
NCT01518036
Use of Somatropin in Turner Syndrometreatment3completed
NCT01710696
Induction of Puberty With 17-beta Estradiol in Girls With Turner Syndrometreatment3completed
NCT01517048
Brain-Derived Neurotrophic Factor in Obesity and Brain FunctionNo drug interventionsNot AvailableNot Availablecompleted
NCT06144957
SLC13A5 Deficiency Natural History Study - United States OnlyNo drug interventionsNot AvailableNot Availablerecruiting
NCT01563926
Evaluating Acceptance of New Liquid Somatropin Formulation in Children With Growth Hormone Deficiencytreatment3completed
NCT01245374
Norditropin NordiFlex® Device Compared to the Device Previously Used by Patients or ParentsNo drug interventionstreatment4completed
NCT03093220
Molecular Typing of Community-acquired Pneumonia Based on Multiple-omic Data AnalysisNo drug interventionsNot AvailableNot Availableunknown_status
NCT01518062
Safety of Somatropin and Induction of Puberty With 17-beta-oestradiol in Girls With Turner Syndrometreatment4completed
NCT01401244
Bioequivalence of Two Somatropin Products (Norditropin® Versus Genotropin®) in Healthy Adult Volunteerstreatment1completed
NCT01529840
Somatropin Effect on Linear Growth and Final Height in Subjects With Noonan Syndrometreatment3completed
NCT01543867
Safety and Efficacy of Long-term Somatropin Treatment in ChildrenNot AvailableNot Availablecompleted
NCT00262288
Recombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary Angioedematreatment2 / 3completed
NCT00578435
Allogeneic Bone Marrow Transplantation for the Treatment of Genetic Disorders of ErythropoiesisNo drug interventionstreatment2completed
NCT00214448
Reproducibility of the Array-Based Comparative Genomic Hybridization (aCGH) System Using Whole Blood SamplesNo drug interventionsNot AvailableNot Availableunknown_status
NCT03911531
Whole Exome Sequencing and Whole Genome Sequencing for Nonimmune Fetal/Neonatal HydropsNo drug interventionsNot AvailableNot Availablerecruiting
NCT01902901
Clinical Implementation of Carrier Status Using Next Generation SequencingNo drug interventionsscreeningNot Availablecompleted
NCT00705055
Face Anthropometric Pattern Recognition Technology for Computer Aided Diagnosis of Human Genetic Disorders.No drug interventionsNot AvailableNot Availablecompleted
NCT00261053
Recombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary Angioedematreatment2completed
NCT00851409
A Study of the Safety and Immunogenicity of Repeated rhC1INH Administrationtreatment2completed
NCT01401257
Phase II, Randomized, Placebo-controlled Trial in Patients With Charcot-marie-tooth Disease Type 1Atreatment2completed
NCT00262301
Recombinant Human C1 Inhibitor for the Treatment of Acute Attacks in Patients With Hereditary Angioedematreatment3completed