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#619690 - BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG
Cytogenetic locations: ##@###
Gene summaries Genetic tests Medical literature
#619657 - CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 8, WITH OR WITHOUT HETEROTAXY; CHTD8
Cytogenetic locations: pb#x##
#619656 - LOEYS-DIETZ SYNDROME 6; LDS6
Cytogenetic locations: 0^#d##
#619538 - CEREBRAL CAVERNOUS MALFORMATIONS 4; CCM4
#619339 - BARTSOCAS-PAPAS SYNDROME 2; BPS2
Cytogenetic locations: 138250
#619281 - IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE; IMD14B
Cytogenetic locations: 1p36.22
#619087 - NOONAN SYNDROME 13; NS13
Cytogenetic locations: 0#{}##
#619030 - SKELETAL MUSCLE GLYCOGEN CONTENT AND METABOLISM QUANTITATIVE TRAIT LOCUS; SMGMQTL
Cytogenetic locations: #y####
#618858 - DIABETES MELLITUS, PERMANENT NEONATAL, 4; PNDM4
Cytogenetic locations: 11p15.5
#618681 - LESSEL-KUBISCH SYNDROME; LSKB
Cytogenetic locations: #d####
#618333 - MENKE-HENNEKAM SYNDROME 2; MKHK2
Cytogenetic locations: 113508
#618332 - MENKE-HENNEKAM SYNDROME 1; MKHK1
Cytogenetic locations: 611002
#618213 - INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY; IBDIMDE
#618204 - IMMUNODEFICIENCY 15A; IMD15A
Cytogenetic locations: 615215
#617691 - SPINOCEREBELLAR ATAXIA 44; SCA44
Cytogenetic locations: ######
#616863 - HAO-FOUNTAIN SYNDROME; HAFOUS
CHROMOSOME 16p13.2 DELETION SYNDROME, INCLUDED
Cytogenetic locations: `~####
#616707 - DEAFNESS, AUTOSOMAL DOMINANT 68; DFNA68
Cytogenetic locations: #P####
#616559 - NOONAN SYNDROME 9; NS9
Cytogenetic locations: #(2###
#616214 - HYPERPROINSULINEMIA
#616171 - MICROCEPHALY AND CHORIORETINOPATHY, AUTOSOMAL RECESSIVE, 2; MCCRP2
Cytogenetic locations: 614161
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