Disorder of protein O-glycosylation
MONDO:0017741A disease that has its basis in the disruption of protein O-linked glycosylation.
Also known as: disorder of protein O-linked glycosylation, protein O-linked glycosylation disease
13 clinical trials for this condition and its sub-types, 0 tagged with Disorder of protein O-glycosylation itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Disorder of protein O-glycosylation
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Myopathy caused by variation in FKRP 0 trials · 8 incl. sub-types
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Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan 0 trials · 8 incl. sub-types
9 sub-types
- Qualitative or quantitative defects of FKRP 0 trials · 8 incl. sub-types Sub-types →
- Myopathy caused by variation in FKTN 1 trial · 2 incl. sub-types Sub-types →
- Myopathy caused by variation in CRPPA 0 trials · 1 incl. sub-types Sub-types →
- Myopathy caused by variation in GMPPB 0 trials · 1 incl. sub-types Sub-types →
- Myopathy caused by variation in POMT1 0 trials · 1 incl. sub-types Sub-types →
- Myopathy caused by variation in POMT2 0 trials · 1 incl. sub-types Sub-types →
- Qualitative or quantitative defects of protein O-mannosyltransferase 1 0 trials · 1 incl. sub-types Sub-types →
- Qualitative or quantitative defects of protein O-mannosyltransferase 2 0 trials · 1 incl. sub-types Sub-types →
- Limb-girdle muscular dystrophy due to POMK deficiency 0 trials
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Disorder of fucoglycosan synthesis 0 trials · 4 incl. sub-types
3 sub-types
- Dowling-Degos disease 0 trials · 4 incl. sub-types Sub-types →
- Peters plus syndrome 0 trials
- Autosomal recessive spondylocostal dysostosis 0 trials Sub-types →
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Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types
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1 sub-type
Most studied deeper sub-types
Dowling-Degos disease 1
(4)
Autosomal recessive limb-girdle muscular dystrophy type 2K
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2M
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2N
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2T
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2U
(1)
Dowling-Degos disease 2
(0)
Dowling-degos disease 3
(0)
Dowling-Degos disease 4
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7
(0)
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8
(0)
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1
(0)
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
(0)
Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2
(0)
Muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4
(0)
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8
(0)
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