autosomal recessive limb-girdle muscular dystrophy type 2Cautosomal recessive limb-girdle muscular dystrophy type 2Dautosomal recessive limb-girdle muscular dystrophy type 2Eautosomal recessive limb-girdle muscular dystrophy type 2Fqualitative or quantitative defects of alpha-sarcoglycanqualitative or quantitative defects of beta-sarcoglycanqualitative or quantitative defects of gamma-sarcoglycanqualitative or quantitative defects of delta-sarcoglycan
P279
Q27677698-cca7f870-49f9-f832-2fe5-1dcd74c3a754Q27677699-f9f15bf5-41ee-76b6-9740-637f5850a855Q27677700-66876eed-42d9-fa6d-1a08-1b3b350ad5faQ27677701-68b936fa-4c93-4774-082d-bc5d4251cf0eQ55785961-DFC07A2D-2C6D-4847-A5D0-C356ABE88DAFQ55785963-4311DE1D-ED62-43CA-B2B1-EF119AF8ECFFQ55785964-7E5D27D4-513F-4778-BE21-A1FA8EBC500BQ55785965-67A3BC96-F1AE-42C6-AFEF-F4AF0F1BE9FF
P279
description
collection of diseases resulting from mutations in any of the four sarcoglycan genes
@en
name
sarcoglicanopatía
@es
sarcoglycanopathie
@fr
sarcoglycanopathy
@en
type
label
sarcoglicanopatía
@es
sarcoglycanopathie
@fr
sarcoglycanopathy
@en
altLabel
qualitative or quantitative defects of sarcoglycan
@en
sarcoglicanopatia
@es
prefLabel
sarcoglicanopatía
@es
sarcoglycanopathie
@fr
sarcoglycanopathy
@en
P672
P486
P6366
P1550
P1995
P279
P2888
P2892
P486
P5270
MONDO:0016140
P6366
2779561866
P672
C05.651.534.500.280.500
C08.618.923
C10.668.491.175.500.149.500
C14.280.238.812
C16.320.577.280.500