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Clinical and Molecular Investigations Into Ciliopathies
This study is currently recruiting participants.
Verified February 2013
by National Institutes of Health Clinical Center (CC)
Study NCT00068224 Information provided by National Institutes of Health Clinical Center (CC)
First Received on September 10, 2003. Last Updated on May 1, 2013
History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Congenital Hepatic Fibrosis
Caroli's Disease
Polycystic Kidney Disease
Joubert Syndrome
Cerebro-Oculo-Renal Syndromes
COACH Syndrome
Senior-Loken Syndrome
Dekaban-Arima Syndrome
Cogan Oculomotor Apraxia
Nephronophthisis
Bardet-Biedl Syndrome
Alstrom Syndrome
Oral-Facial-Digital Syndrome
Additional conditions recognized in this trial
Abnormalities, Multiple
Apraxias
Ataxia
Caroli Disease
Cerebellar Diseases
Cholestasis
Cogan Syndrome
Coloboma
Coma
Cysts
Eye Abnormalities
Fibrosis
Kidney Diseases
Kidney Diseases, Cystic
Laurence-Moon Syndrome
Leber Congenital Amaurosis
Liver Cirrhosis
Liver Diseases
Oculocerebrorenal Syndrome
Optic Atrophies, Hereditary
Orofaciodigital Syndromes
Polycystic Kidney Diseases
Polycystic Kidney, Autosomal Recessive
More general conditions related to this trial
Amino Acid Transport Disorders, Inborn
Bile Duct Diseases
Biliary Tract Diseases
Bone Diseases
Bone Diseases, Developmental
Brain Diseases
Brain Diseases, Metabolic
Brain Diseases, Metabolic, Inborn
Cardiovascular Diseases
Central Nervous System Diseases
Choledochal Cyst
Chromosome Disorders
Congenital Abnormalities
Consciousness Disorders
Cranial Nerve Diseases
Craniofacial Abnormalities
Digestive System Abnormalities
Digestive System Diseases
Dyskinesias
Dysostoses
Eye Diseases
Eye Diseases, Hereditary
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Hereditary Sensory and Motor Neuropathy
Heredodegenerative Disorders, Nervous System
Hypothalamic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Musculoskeletal Abnormalities
Musculoskeletal Diseases
Neoplasms
Nervous System Diseases
Nervous System Malformations
Neurobehavioral Manifestations
Neurodegenerative Diseases
Neurologic Manifestations
Neuromuscular Diseases
Optic Atrophy
Optic Nerve Diseases
Pathologic Processes
Pathological Conditions, Anatomical
Peripheral Nervous System Diseases
Polyneuropathies
Psychomotor Disorders
Renal Tubular Transport, Inborn Errors
Retinal Diseases
Retinitis Pigmentosa
Sex Chromosome Disorders
Signs and Symptoms
Unconsciousness
Urologic Diseases
Vascular Diseases
Vasculitis
Vestibulocochlear Nerve Diseases
Sponsors listed in this trial
National Human Genome Research Institute (NHGRI)
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