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#311250 - ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO
Cytogenetic locations: Prps2
Gene summaries Genetic tests Medical literature
#603471 - CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2
#312750 - RETT SYNDROME; RTT
RETT SYNDROME, ZAPPELLA VARIANT, INCLUDED
#308800 - KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED; KFSDX
Cytogenetic locations: 601987
*305900 - GLUCOSE-6-PHOSPHATE DEHYDROGENASE; G6PD
*300461 - ORNITHINE CARBAMOYLTRANSFERASE; OTC
*300377 - DYSTROPHIN; DMD
APO-DYSTROPHIN 1, INCLUDED
Cytogenetic locations: Pudp
#237300 - CARBAMOYL PHOSPHATE SYNTHETASE I DEFICIENCY, HYPERAMMONEMIA DUE TO
#222700 - LYSINURIC PROTEIN INTOLERANCE; LPI
Cytogenetic locations: `$#M##
#220110 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 1; MC4DN1
Cytogenetic locations: Usp20
#215700 - CITRULLINEMIA, CLASSIC
#207900 - ARGININOSUCCINIC ACIDURIA
#207800 - ARGININEMIA
#118200 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B
Cytogenetic locations: #o####
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