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#619690 - BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG
Cytogenetic locations: ##@###
Gene summaries Genetic tests Medical literature
#618786 - IMAGAWA-MATSUMOTO SYNDROME; IMMAS
Cytogenetic locations: ######
*616775 - ZINC FINGER PROTEIN 683; ZNF683
Cytogenetic locations: ########d#R#
#615849 - CULLER-JONES SYNDROME; CJS
Cytogenetic locations: 620553
#614116 - NEUROPATHY, HEREDITARY SENSORY, TYPE IE; HSN1E
Cytogenetic locations: #h|###
*613840 - ZINC FINGER PROTEIN 304; ZNF304
#613750 - RETINITIS PIGMENTOSA 27; RP27
RETINAL DEGENERATION, AUTOSOMAL RECESSIVE, CLUMPED PIGMENT TYPE, INCLUDED
#612370 - HYPOGONADOTROPIC HYPOGONADISM 5 WITH OR WITHOUT ANOSMIA; HH5
Cytogenetic locations: 603001
#610829 - HOLOPROSENCEPHALY 9; HPE9
#610227 - SEBORRHEA-LIKE DERMATITIS WITH PSORIASIFORM ELEMENTS
Cytogenetic locations: 605828
*610226 - ZINC FINGER PROTEIN 750; ZNF750
*608892 - CHROMODOMAIN HELICASE DNA-BINDING PROTEIN 7; CHD7
*606245 - SUZ12 POLYCOMB REPRESSIVE COMPLEX 2 SUBUNIT; SUZ12
JJAZ1/JAZF1 FUSION GENE, INCLUDED
*604599 - EUCHROMATIC HISTONE-LYSINE N-METHYLTRANSFERASE 2; EHMT2
*604517 - PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-GAMMA, COACTIVATOR 1, ALPHA; PPARGC1A
*604396 - SET DOMAIN PROTEIN, BIFURCATED, 1; SETDB1
Cytogenetic locations: 159552
#604121 - CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT; ADCADN
*603423 - PR DOMAIN-CONTAINING PROTEIN 1; PRDM1
#602482 - AXENFELD-RIEGER SYNDROME, TYPE 3; RIEG3
*602402 - FORKHEAD BOX C2; FOXC2
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