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*620649 - PHOSPHOLIPASE A2, GROUP IVE; PLA2G4E
Gene summaries Genetic tests Medical literature
#620514 - IMMUNE DYSREGULATION, AUTOIMMUNITY, AND AUTOINFLAMMATION; IDAA
Cytogenetic locations: `#####
#620458 - AURICULOCONDYLAR SYNDROME 2B; ARCND2B
Cytogenetic locations: P##A##
#620352 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 31B; DEE31B
Cytogenetic locations: #T@##
#619947 - WAARDENBURG SYNDROME, TYPE 2F; WS2F
Cytogenetic locations: 0,#_##
#619802 - IMMUNODEFICIENCY 97 WITH AUTOINFLAMMATION; IMD97
#619651 - NEURODEVELOPMENTAL DISORDER WITH HYPERKINETIC MOVEMENTS AND DYSKINESIA; NEDHYD
Cytogenetic locations: 601199
#619647 - DYSKINESIA WITH OROFACIAL INVOLVEMENT, AUTOSOMAL RECESSIVE; DSKOR
#619538 - CEREBRAL CAVERNOUS MALFORMATIONS 4; CCM4
#619407 - WHIM SYNDROME 2; WHIMS2
Cytogenetic locations: P#####
#619381 - IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION; IMD82
Cytogenetic locations: 600488
#619311 - HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS
Cytogenetic locations: #e#>##
#619281 - IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE; IMD14B
Cytogenetic locations: 1p36.22
#619087 - NOONAN SYNDROME 13; NS13
Cytogenetic locations: 0#{}##
#618961 - SPONDYLOMETAPHYSEAL DYSPLASIA WITH CORNEAL DYSTROPHY; SMDCD
Cytogenetic locations: B3gat3
#618922 - NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES; NEDSHBA
Cytogenetic locations: max
#618858 - DIABETES MELLITUS, PERMANENT NEONATAL, 4; PNDM4
Cytogenetic locations: 11p15.5
#618727 - ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB
Cytogenetic locations: #6####
#618624 - NOONAN SYNDROME 12; NS12
Cytogenetic locations: #"####
#618499 - NOONAN SYNDROME 11; NS11
Cytogenetic locations: @##K##
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