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#620343 - BASAL CELL NEVUS SYNDROME 2; BCNS2
Cytogenetic locations: 600664
Gene summaries Genetic tests Medical literature
#620071 - BIRK-AHARONI SYNDROME; BKAH
Cytogenetic locations: #1q}##
#620038 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, HYPOTONIA, AND ABSENT LANGUAGE; NEDMHAL
#619354 - DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP
Cytogenetic locations: assignment
#619239 - NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISM OR SEIZURES; NEDAUS
Cytogenetic locations: ######
#619175 - PROTEASOME-ASSOCIATED AUTOINFLAMMATORY SYNDROME 5; PRAAS5
Cytogenetic locations: 0#w\##
#619102 - SPERMATOGENIC FAILURE 47; SPGF47
#618829 - NABAIS SA-DE VRIES SYNDROME, TYPE 2; NSDVS2
Cytogenetic locations: `#####
#618828 - NABAIS SA-DE VRIES SYNDROME, TYPE 1; NSDVS1
Cytogenetic locations: #7#+##
#618123 - POLYDACTYLY, POSTAXIAL, TYPE A8; PAPA8
Cytogenetic locations: 0W####
*617858 - PROTEASOME INHIBITOR SUBUNIT 1; PSMF1
Cytogenetic locations: -
*617857 - PROTEASOME 26S SUBUNIT, NON-ATPase, 6; PSMD6
Cytogenetic locations: 620561
*617844 - PROTEASOME 26S SUBUNIT, NON-ATPase, 8; PSMD8
Cytogenetic locations: ############
*617842 - PROTEASOME 26S SUBUNIT, NON-ATPase, 1; PSMD1
Cytogenetic locations: #########FV#
*617841 - PROTEASOME SUBUNIT, ALPHA-TYPE, 8; PSMA8
Cytogenetic locations: Cetn1
#617757 - JOUBERT SYNDROME 32; JBTS32
*617676 - PROTEASOME 26S SUBUNIT, NON-ATPase, 3; PSMD3
Cytogenetic locations: ########b,##
#617642 - POLYDACTYLY, POSTAXIAL, TYPE A7; PAPA7
*617632 - EF-HAND CALCIUM-BINDING DOMAIN-CONTAINING PROTEIN 7; EFCAB7
*617631 - IQ DOMAIN-CONTAINING PROTEIN E; IQCE
Cytogenetic locations: @~#7##
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