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#620601 - GARG-MISHRA PROGEROID SYNDROME; GMPGS
Cytogenetic locations: Etv1
Gene summaries Genetic tests Medical literature
*619822 - BCL2-LIKE 13; BCL2L13
Cytogenetic locations: 605938
#618732 - POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS
Cytogenetic locations: OTF3L
#618624 - NOONAN SYNDROME 12; NS12
Cytogenetic locations: #"####
#618499 - NOONAN SYNDROME 11; NS11
Cytogenetic locations: @##K##
#618287 - AUTOINFLAMMATORY DISEASE, FAMILIAL, BEHCET-LIKE 3; AIFBL3
#618165 - BONE MARROW FAILURE SYNDROME 5; BMFS5
#617900 - ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED (HERPES-SPECIFIC), SUSCEPTIBILITY TO, 8; IIAE8
Cytogenetic locations: slightly
#617584 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 25; SCAR25
#617306 - COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD
Cytogenetic locations: #C#l##
#617158 - MYOPATHY, DISTAL, WITH RIMMED VACUOLES; DMRV
Cytogenetic locations: 5q35.3
#617145 - NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET; NADGP
#617087 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B
Cytogenetic locations: 1p36.22
#617062 - OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS
Cytogenetic locations: 19q13.42
#616937 - THROMBOCYTOPENIA 6; THC6
Cytogenetic locations: #####
*616659 - TBC1 DOMAIN FAMILY, MEMBER 17; TBC1D17
#616439 - FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 4; FTDALS4
#616437 - FRONTOTEMPORAL DEMENTIA AND/OR AMYOTROPHIC LATERAL SCLEROSIS 3; FTDALS3
*615687 - BECLIN 2; BECN2
Cytogenetic locations: Zona
#615278 - CARDIOFACIOCUTANEOUS SYNDROME 2; CFC2
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