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Telomere syndrome

MONDO:0100137

Accelerated aging syndromes often caused by inheritable gene mutations resulting in decreased telomere lengths.

Also known as: STS, short telomere syndrome

80 clinical trials for this condition and its sub-types.

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Sub-types

Primary biliary cholangitis (63) Cirrhosis, familial (3) Nodular regenerative hyperplasia of the liver (3) Isolated congenital hepatic fibrosis (2) Immunodeficiency-centromeric instability-facial anomalies syndrome (1) Primary biliary cholangitis 1 (1) Pulmonary fibrosis and/or bone marrow failure, telomere-related (1) ACD-related long telomere syndrome (0) ACD-related short telomere syndrome (0) ACD-related telomere biology disorder (0) Cerebroretinal microangiopathy with calcifications and cysts 1 (0) Cerebroretinal microangiopathy with calcifications and cysts 2 (0) Cerebroretinal microangiopathy with calcifications and cysts 3 (0) Cirrhosis, familial, with antigenemia (0) Coats plus syndrome (0) Dyskeratosis congenita, autosomal dominant 1 (0) Dyskeratosis congenita, autosomal dominant 6 (0) Dyskeratosis congenita, autosomal recessive 7 (0) Immunodeficiency-centromeric instability-facial anomalies syndrome 1 (0) Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (0)

Broader categories

Disease (618) Human disease (14) Premature aging syndrome (6) Disease by developmental or physiological process (0)
Trials to join now! 32 Not yet recruiting 11 Not yet finished but already full! 18 Completed 16 Terminated 3
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