Glycoprotein metabolism disease
MONDO:0045010A disease that has its basis in the disruption of glycoprotein metabolic process.
Also known as: disorder of glycoprotein metabolic process, disorder of glycoprotein metabolism, glycoprotein metabolic process disease, glycoprotein metabolism disease
23 clinical trials for this condition and its sub-types, 1 tagged with Glycoprotein metabolism disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Glycoprotein metabolism disease
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Disorder of protein O-glycosylation 0 trials · 13 incl. sub-types
6 sub-types
- Myopathy caused by variation in FKRP 0 trials · 8 incl. sub-types Sub-types →
- Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan 0 trials · 8 incl. sub-types Sub-types →
- Disorder of fucoglycosan synthesis 0 trials · 4 incl. sub-types Sub-types →
- Autosomal recessive limb-girdle muscular dystrophy type 2R1 1 trial
- Myopathy caused by variation in POMGNT1 0 trials · 1 incl. sub-types Sub-types →
- Myopathy caused by variation in POMGNT2 0 trials Sub-types →
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Disorder of protein N-glycosylation 0 trials · 7 incl. sub-types
26 sub-types
- PMM2-congenital disorder of glycosylation 5 trials
- MPI-congenital disorder of glycosylation 1 trial
- PGM1-congenital disorder of glycosylation 1 trial
- ALG1-congenital disorder of glycosylation 0 trials
- ALG11-congenital disorder of glycosylation 0 trials
- ALG12-congenital disorder of glycosylation 0 trials
- ALG2-congenital disorder of glycosylation 0 trials Sub-types →
- ALG3-congenital disorder of glycosylation 0 trials
- ALG6-congenital disorder of glycosylation 1C 0 trials
- ALG8-congenital disorder of glycosylation 0 trials
- ALG9-congenital disorder of glycosylation 0 trials Sub-types →
- DDOST-congenital disorder of glycosylation 0 trials
- DPAGT1-congenital disorder of glycosylation 0 trials
- MAN1B1-congenital disorder of glycosylation 0 trials
- MGAT2-congenital disorder of glycosylation 0 trials
- MOGS-congenital disorder of glycosylation 0 trials
- RFT1-congenital disorder of glycosylation 0 trials
- SLC39A8-CDG 0 trials
- SSR4-congenital disorder of glycosylation 0 trials
- ST3GAL3-congenital disorder of glycosylation 0 trials Sub-types →
- STT3A-congenital disorder of glycosylation 0 trials
- STT3B-congenital disorder of glycosylation 0 trials
- TMEM165-congenital disorder of glycosylation 0 trials
- Autism spectrum disorder - epilepsy - arthrogryposis syndrome 0 trials
- Congenital disorder of glycosylation type 1EE with or without immunodeficiency 0 trials
- Developmental and epileptic encephalopathy, 36 0 trials
Most studied deeper sub-types
Autosomal recessive limb-girdle muscular dystrophy type 2I
(8)
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 2O
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2T
(1)
Autosomal recessive limb-girdle muscular dystrophy type 2U
(1)
Myopathy caused by variation in FKTN
(1)
Autosomal recessive spondylocostal dysostosis
(0)
Congenital muscular dystrophy caused by variation in POMGNT2
(0)
Congenital myasthenic syndrome 14
(0)
Developmental and epileptic encephalopathy, 15
(0)
Dowling-Degos disease
(0)
Dowling-Degos disease 2
(0)
Dowling-degos disease 3
(0)
Dowling-Degos disease 4
(0)
Gillessen-Kaesbach-Nishimura syndrome
(0)
Intellectual disability, autosomal recessive 12
(0)
Limb-girdle muscular dystrophy due to POMK deficiency
(0)