Familial osteosclerosis
MONDO:0042973An 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, 0 tagged with Familial osteosclerosis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Familial osteosclerosis
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Osteopetrosis 6 trials · 14 incl. sub-types
11 sub-types
- Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome 4 trials
- Melorheostosis 3 trials
- Autosomal recessive osteopetrosis 0 trials · 2 incl. sub-types Sub-types →
- Autosomal dominant osteopetrosis 0 trials Sub-types →
- Dysosteosclerosis 0 trials
- Early-onset calcifying leukoencephalopathy-skeletal dysplasia 0 trials
- Infantile osteopetrosis with neuroaxonal dysplasia 0 trials Sub-types →
- Osteomesopyknosis 0 trials
- Osteopathia striata with cranial sclerosis 0 trials
- Osteosclerotic metaphyseal dysplasia 0 trials
- Pycnodysostosis 0 trials
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Craniometaphyseal dysplasia 1 trial · 2 incl. sub-types
4 sub-types
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Axial osteomalacia 0 trials
Most studied deeper sub-types
Autosomal recessive osteopetrosis 1
(1)
Autosomal recessive osteopetrosis 2
(1)
Autosomal dominant osteopetrosis 1
(0)
Autosomal dominant osteopetrosis 2
(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)
Leukocyte adhesion deficiency 3
(0)
Osteopetrosis, autosomal dominant 3
(0)
Osteopetrosis, autosomal dominant 4
(0)
Osteopetrosis, autosomal recessive 9
(0)
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