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#620745 - DEAFNESS, AUTOSOMAL RECESSIVE 123; DFNB123
Gene summaries Genetic tests Medical literature
#618858 - DIABETES MELLITUS, PERMANENT NEONATAL, 4; PNDM4
Cytogenetic locations: 11p15.5
#618782 - LONG QT SYNDROME 16; LQT16
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC 6, INCLUDED; CPVT6, INCLUDED
Cytogenetic locations: pJVU##
#618760 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS; NEDHAHM
#617665 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 56; DEE56
#616249 - LONG QT SYNDROME 15; LQT15
#616247 - LONG QT SYNDROME 14; LQT14
#616214 - HYPERPROINSULINEMIA
#616087 - TYPE 2 DIABETES 5; T2D5
#615109 - COWDEN SYNDROME 6; CWS6
Cytogenetic locations: GSKIP
#614916 - VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4; CPVT4
Cytogenetic locations: ######
#613370 - MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 10; MODY10
Cytogenetic locations: ##Y###
*612465 - TBC1 DOMAIN FAMILY, MEMBER 4; TBC1D4
Cytogenetic locations: -
#611742 - SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 9; SHEP9
#611556 - GLYCOGEN STORAGE DISEASE 0, MUSCLE; GSD0B
Cytogenetic locations: distal
#610549 - DIABETES MELLITUS, INSULIN-RESISTANT, WITH ACANTHOSIS NIGRICANS
Cytogenetic locations: #<#&##
*610415 - SYNTAXIN-BINDING PROTEIN 4; STXBP4
Cytogenetic locations: ?Atrial
#609968 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 5; HHF5
*609009 - TYROSINE 3-MONOOXYGENASE/TRYPTOPHAN 5-MONOOXYGENASE ACTIVATION PROTEIN, THETA ISOFORM; YWHAQ
Cytogenetic locations: #########9##
*605857 - RAS HOMOLOG GENE FAMILY, MEMBER Q; RHOQ
Cytogenetic locations: #########W##
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