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MIM:606407 - HYPOTONIA-CYSTINURIA SYNDROME
Xenbase Genes: slc3a1, prepl
Human Disease Resource: MIM
MONDO:0011669 - hypotonia-cystinuria syndrome |
MONDO:0015583 - 2p21 microdeletion syndrome |
MONDO:0016539 - atypical hypotonia-cystinuria syndrome |
DOID:0060858 - hypotonia-cystinuria syndrome |