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*620520 - CALMODULIN-LIKE 4; CALML4
Cytogenetic locations: 607856
Gene summaries Genetic tests Medical literature
#620430 - AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 3; ADMIO3
Cytogenetic locations: -
#619864 - LEUKODYSTROPHY, CHILDHOOD-ONSET, REMITTING; CORLK
#619680 - MARBACH-SCHAAF NEURODEVELOPMENTAL SYNDROME; MASNS
Cytogenetic locations: p#N###
#619614 - RETINITIS PIGMENTOSA 92; RP92
Cytogenetic locations: 600438
*619540 - PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 3E; PPP1R3E
Cytogenetic locations: 613457
#619538 - CEREBRAL CAVERNOUS MALFORMATIONS 4; CCM4
#619375 - AUTOINFLAMMATORY SYNDROME, FAMILIAL, WITH OR WITHOUT IMMUNODEFICIENCY; AISIMD
Cytogenetic locations: 16p13.3
#619281 - IMMUNODEFICIENCY 14B, AUTOSOMAL RECESSIVE; IMD14B
Cytogenetic locations: 1p36.22
#619143 - CARDIOACROFACIAL DYSPLASIA 2; CAFD2
Cytogenetic locations: `#####
#619142 - CARDIOACROFACIAL DYSPLASIA 1; CAFD1
Cytogenetic locations: PwU###
#619087 - NOONAN SYNDROME 13; NS13
Cytogenetic locations: 0#{}##
#619072 - NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND BRAIN ATROPHY; NEDSEBA
#619030 - SKELETAL MUSCLE GLYCOGEN CONTENT AND METABOLISM QUANTITATIVE TRAIT LOCUS; SMGMQTL
Cytogenetic locations: #y####
#619016 - IFAP SYNDROME 2; IFAP2
Cytogenetic locations: PER1
#618858 - DIABETES MELLITUS, PERMANENT NEONATAL, 4; PNDM4
Cytogenetic locations: 11p15.5
#618782 - LONG QT SYNDROME 16; LQT16
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC 6, INCLUDED; CPVT6, INCLUDED
Cytogenetic locations: pJVU##
#618547 - NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES; NEDVIBA
Cytogenetic locations: ######
#618204 - IMMUNODEFICIENCY 15A; IMD15A
Cytogenetic locations: 615215
#617506 - NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR 2; NSLH2
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