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#619880 - NEURODEVELOPMENTAL DISORDER WITH POOR GROWTH AND SKELETAL ANOMALIES; NEDGS
Cytogenetic locations: 34244665
Gene summaries Genetic tests Medical literature
*606306 - PROTOCADHERIN-GAMMA, SUBFAMILY C, MEMBER 5; PCDHGC5
Cytogenetic locations: 5q31.2
*606305 - PROTOCADHERIN-GAMMA, SUBFAMILY C, MEMBER 4; PCDHGC4
Cytogenetic locations: opposite
*606304 - PROTOCADHERIN-GAMMA, SUBFAMILY B, MEMBER 7; PCDHGB7
Cytogenetic locations: 11230163
*606303 - PROTOCADHERIN-GAMMA, SUBFAMILY B, MEMBER 6; PCDHGB6
*606302 - PROTOCADHERIN-GAMMA, SUBFAMILY B, MEMBER 5; PCDHGB5
*606301 - PROTOCADHERIN-GAMMA, SUBFAMILY B, MEMBER 3; PCDHGB3
*606300 - PROTOCADHERIN-GAMMA, SUBFAMILY B, MEMBER 2; PCDHGB2
*606299 - PROTOCADHERIN-GAMMA, SUBFAMILY B, MEMBER 1; PCDHGB1
Cytogenetic locations: 609372
*606298 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 11; PCDHGA11
Cytogenetic locations: Amyotrophic
*606297 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 10; PCDHGA10
*606296 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 9; PCDHGA9
*606295 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 8; PCDHGA8
Cytogenetic locations: Even-plus
*606294 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 7; PCDHGA7
*606293 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 6; PCDHGA6
*606292 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 5; PCDHGA5
Cytogenetic locations: mutation
*606291 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 4; PCDHGA4
Cytogenetic locations: 609373
*606290 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 3; PCDHGA3
Cytogenetic locations: CDC25C
*606289 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 2; PCDHGA2
*606288 - PROTOCADHERIN-GAMMA, SUBFAMILY A, MEMBER 1; PCDHGA1
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