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Search in Field(s): clear
Title MIM number Allelic Variants .
.
Text References Clinical Synopsis
Gene Map Disorder Contributors .
.
Chromosome(s): clear
1 2 3 4 5 6 7 8 .
.
9 10 11 12 13 14 15 16
17 18 19 20 21 22 X Y .
.
mitochondrial unknown .
.
MIM Number Prefix: clear
* gene with known sequence
+ gene with known sequence
and phenotype
# phenotype description,
molecular basis known
% mendelian phenotype or locus,
molecular basis unknown
none other, mainly phenotypes with
suspected mendelian basis
Only Records with: clear
Allelic Variants
Clinical Synopsis
Gene map locus
 
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