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#612337 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 22; MRD22
CHROMOSOME 1q43-q44 DELETION SYNDROME, INCLUDED
Cytogenetic locations: 22095278
Gene summaries Genetic tests Medical literature
%612433 - DEAFNESS, AUTOSOMAL RECESSIVE 45; DFNB45
Cytogenetic locations: MAP3K21
*608433 - ZINC FINGER- AND BTB DOMAIN-CONTAINING PROTEIN 18; ZBTB18
Cytogenetic locations: 20059953
#615937 - MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 2; MPPH2
Cytogenetic locations: 22729224
*604934 - TUBULIN-SPECIFIC CHAPERONE E; TBCE
Cytogenetic locations: 18706133
#603387 - MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 1; MPPH1
Cytogenetic locations: 17675034
%217990 - CORPUS CALLOSUM, AGENESIS OF
*613524 - SHH SIGNALING AND CILIOGENESIS REGULATOR SDCCAG8; SDCCAG8
Cytogenetic locations: 612433
*606416 - NLR FAMILY, PYRIN DOMAIN-CONTAINING 3; NLRP3
Cytogenetic locations: 21124315
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