- Diseases
- Mucopolysaccharidosis type 7
Mucopolysaccharidosis type 7
Name: |
Mucopolysaccharidosis type 7
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Description: |
A rare, genetic lysosomal storage disease characterized by accumulation of glycosaminoglycans in connective tissue which results in progressive multisystem involvement with severity ranging from mild to severe. The most consistent features include musculoskeletal involvement (particularly dysostosis multiplex, joint restriction, thorax abnormalities, and short stature), limited vocabulary, intellectual disability, coarse facies with a short neck, pulmonary involvement (predominantly decreased pulmonary function), corneal clouding, and cardiac valve disease.
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ORPHAcode: |
584
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Synonyms: |
Beta-glucuronidase deficiency
MPS7
MPSVII
Mucopolysaccharidosis type VII
Sly disease
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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Lysomal Storage (64 genes) - VUB
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ADCY5 94.52 0 No comment AGA 100.00 0 No comment ARSA 100.00 0 No comment SLURP1 85.73 0 No comment ASAH1 99.94 0 No comment CHIT1 100.00 0 No comment CLN3 100.00 0 No comment CLN5 99.94 0 No comment CLN6 90.35 0 No comment CLN8 100.00 0 No comment CTNS 100.00 0 No comment CTSA 100.00 0 No comment CTSC 100.00 0 No comment CTSD 99.45 0 No comment CTSK 100.00 0 No comment DGUOK 100.00 0 No comment FBXL4 100.00 0 No comment FUCA1 100.00 0 No comment GAA 100.00 0 No comment GALC 98.44 0 No comment GALNS 96.18 0 No comment GBA1 100.00 0 No comment GLA 100.00 0 No comment GLB1 100.00 0 No comment GM2A 100.00 0 No comment GNPTAB 100.00 0 No comment GNPTG 94.69 0 No comment GNS 100.00 0 No comment GUSB 100.00 0 No comment HEXA 100.00 0 No comment HEXB 99.82 0 No comment HGSNAT 93.95 0 No comment HYAL1 100.00 0 No comment IDS 100.00 0 No comment IDUA 88.67 0 No comment LAMP2 100.00 0 No comment LIPA 100.00 0 No comment MAN2B1 100.00 0 No comment MANBA 99.97 0 No comment MCOLN1 97.27 0 No comment MFSD8 100.00 0 No comment MGME1 100.00 0 No comment MPV17 100.00 0 No comment NAGA 100.00 0 No comment NAGLU 87.38 0 No comment NEU1 100.00 0 No comment NPC1 98.40 0 No comment NPC2 100.00 0 No comment OCRL 99.77 0 No comment POLG 100.00 0 No comment PPT1 100.00 0 No comment PSAP 100.00 0 No comment RRM2B 100.00 0 No comment SGSH 99.99 0 No comment SLC17A5 100.00 0 No comment SMPD1 100.00 0 No comment STS 100.00 0 No comment SUCLA2 100.00 0 No comment SUCLG1 95.74 0 No comment SUMF1 100.00 0 No comment TK2 95.90 0 No comment ACD 100.00 0 No comment TWNK 100.00 0 No comment TYMP 91.72 0 No comment -
Metabolic diseases with hepatic disorders (20 genes) - UCL
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments ATP7B 100.00 1 Part of Custom Gastro-pneumo panel CPT1A 100.00 1 Part of Custom Gastro-pneumo panel CYP27A1 100.00 1 Part of Custom Gastro-pneumo panel DGUOK 100.00 1 Part of Custom Gastro-pneumo panel DHCR7 100.00 1 Part of Custom Gastro-pneumo panel EHHADH 100.00 1 Part of Custom Gastro-pneumo panel GBE1 100.00 1 Part of Custom Gastro-pneumo panel GNAS 0.00 1 Part of Custom Gastro-pneumo panel / only Exons 8 and 9 GUSB 100.00 1 Part of Custom Gastro-pneumo panel LIPA 100.00 1 Part of Custom Gastro-pneumo panel MPV17 100.00 1 Part of Custom Gastro-pneumo panel NEU1 100.00 1 Part of Custom Gastro-pneumo panel NPC1 100.00 1 Part of Custom Gastro-pneumo panel NPC2 100.00 1 Part of Custom Gastro-pneumo panel POLG 100.00 1 Part of Custom Gastro-pneumo panel SI 100.00 1 Part of Custom Gastro-pneumo panel SLC25A13 100.00 1 Part of Custom Gastro-pneumo panel SMPD1 100.00 1 Part of Custom Gastro-pneumo panel TALDO1 100.00 1 Part of Custom Gastro-pneumo panel TRMU 100.00 1 Part of Custom Gastro-pneumo panel