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Familial osteosclerosis

MONDO:0042973

An instance of osteosclerosis that is caused by an inherited modification of the individual's genome.

Also known as: hereditary osteosclerosis

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

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Sub-types

Osteopetrosis (6) Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome (4) Melorheostosis (3) Autosomal recessive osteopetrosis 1 (1) Autosomal recessive osteopetrosis 2 (1) Craniometaphyseal dysplasia (1) Craniometaphyseal dysplasia, autosomal dominant (1) Autosomal dominant osteopetrosis (0) Autosomal dominant osteopetrosis 1 (0) Autosomal dominant osteopetrosis 2 (0) Autosomal recessive osteopetrosis (0) Autosomal recessive osteopetrosis 3 (0) Autosomal recessive osteopetrosis 4 (0) Autosomal recessive osteopetrosis 5 (0) Autosomal recessive osteopetrosis 6 (0) Autosomal recessive osteopetrosis 7 (0) Autosomal recessive osteopetrosis 8 (0) Axial osteomalacia (0) Craniodiaphyseal dysplasia (0) Craniodiaphyseal dysplasia, autosomal dominant (0)

Broader categories

Disease (717) Musculoskeletal system disorder (214) Hereditary disease (188) Bone disorder (51) Human disease (15) Bone remodeling disease (5) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Osteosclerosis (1) Disease by body system or component (0)
Trials to join now! 8 Not yet recruiting 1 Not yet finished but already full! 2 Completed 5
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