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611886 - MESOMELIC DYSPLASIA, CAMERA TYPE
Gene summaries Genetic tests Medical literature
#620606 - SPASTIC PARAPLEGIA 72B, AUTOSOMAL RECESSIVE; SPG72B
#615040 - EPISODIC PAIN SYNDROME, FAMILIAL, 1; FEPS1
Cytogenetic locations: between
%221800 - DERMOCHONDROCORNEAL DYSTROPHY
#614546 - EFAVIRENZ, POOR METABOLISM OF
EFAVIRENZ CENTRAL NERVOUS SYSTEM TOXICITY, SUSCEPTIBILITY TO, INCLUDED
Cytogenetic locations: 15194512
%167730 - NASOPALPEBRAL LIPOMA-COLOBOMA SYNDROME; NPLCS
#615625 - SPASTIC PARAPLEGIA 72A, AUTOSOMAL DOMINANT; SPG72A
Cytogenetic locations: 5q31.1
#609195 - SPASTIC PARAPLEGIA 26, AUTOSOMAL RECESSIVE; SPG26
Cytogenetic locations: 15635080
*604735 - UBIQUITIN-SPECIFIC PROTEASE 16; USP16
Cytogenetic locations: 20170901
*617059 - ZINC FINGER DBF DOMAIN-CONTAINING PROTEIN 2; ZDBF2
LONG ISOFORM OF ZDBF2, INCLUDED; LIZ, INCLUDED
Cytogenetic locations: 601951
*126337 - DNA DAMAGE-INDUCIBLE TRANSCRIPT 3; DDIT3
CHOP/FUS FUSION GENE, INCLUDED
Cytogenetic locations: 11547942
*615790 - AT-HOOK DNA-BINDING MOTIF-CONTAINING PROTEIN 1; AHDC1
Cytogenetic locations: 608042
*613018 - TYROSINE AMINOTRANSFERASE; TAT
Cytogenetic locations: 22859594
#615829 - XIA-GIBBS SYNDROME; XIGIS
*601873 - BETA-1,4-N-ACETYLGALACTOSAMINYLTRANSFERASE 1; B4GALNT1
Cytogenetic locations: 18855236
*131310 - ENGRAILED 2; EN2
Cytogenetic locations: 17015829
*300008 - CHLORIDE CHANNEL 5; CLCN5
Cytogenetic locations: 19131966
*603612 - TUMOR NECROSIS FACTOR RECEPTOR SUPERFAMILY, MEMBER 10B; TNFRSF10B
Cytogenetic locations: 19326928
#613684 - RUBINSTEIN-TAYBI SYNDROME 2; RSTS2
Cytogenetic locations: 22q11.21
*609347 - RECEPTOR EXPRESSION-ENHANCING PROTEIN 2; REEP2
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