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*620520 - CALMODULIN-LIKE 4; CALML4
Cytogenetic locations: 607856
Gene summaries Genetic tests Medical literature
#620475 - THROMBOCYTOPENIA 8, WITH DYSMORPHIC FEATURES AND DEVELOPMENTAL DELAY; THC8
Cytogenetic locations: ##H###
#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
#619271 - BLEEDING DISORDER, PLATELET-TYPE, 24; BDPLT24
Cytogenetic locations: between
#619267 - GLANZMANN THROMBASTHENIA 2; GT2
#618987 - IMMUNODEFICIENCY 73C WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND HYPOGAMMAGLOBULINEMIA; IMD73C
Cytogenetic locations: HCHGQ3
#618986 - IMMUNODEFICIENCY 73B WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND LYMPHOPENIA; IMD73B
#618963 - IMMUNODEFICIENCY 69; IMD69
Cytogenetic locations: 107770
#618782 - LONG QT SYNDROME 16; LQT16
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC 6, INCLUDED; CPVT6, INCLUDED
Cytogenetic locations: pJVU##
#618727 - ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB
Cytogenetic locations: #6####
#618577 - NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES; NEDBAF
#618287 - AUTOINFLAMMATORY DISEASE, FAMILIAL, BEHCET-LIKE 3; AIFBL3
#618204 - IMMUNODEFICIENCY 15A; IMD15A
Cytogenetic locations: 615215
#618165 - BONE MARROW FAILURE SYNDROME 5; BMFS5
#617751 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 48; MRD48
#617744 - IMMUNODEFICIENCY, DEVELOPMENTAL DELAY, AND HYPOHOMOCYSTEINEMIA; IMDDHH
Cytogenetic locations: #$#E##
#617572 - EXUDATIVE VITREORETINOPATHY 7; EVR7
Cytogenetic locations: 0#####
#617523 - NEURODEVELOPMENTAL DISORDER WITH MIDBRAIN AND HINDBRAIN MALFORMATIONS; NEDMHM
Cytogenetic locations: YY1AP1
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