OMIM Links for Protein (Select 25014053) - OMIM - NCBI

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Links from Protein

Items: 1 to 20 of 49

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Select item 6199271.

#619927 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 67; MRD67

Cytogenetic locations: Spinocerebellar

OMIM:: 619927

Gene summaries Genetic tests Medical literature

Select item 6189242.

#618924 - EPISODIC ATAXIA, TYPE 9; EA9

Cytogenetic locations: 23550958

OMIM:: 618924

Gene summaries Genetic tests Medical literature

Select item 6189063.

#618906 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS

Cytogenetic locations: 31616000

OMIM:: 618906

Gene summaries Genetic tests Medical literature

Select item 6185484.

#618548 - MULTIPLE CONGENITAL ANOMALIES-HYPOTONIA-SEIZURES SYNDROME 4; MCAHS4

Cytogenetic locations: 31148362

OMIM:: 618548

Gene summaries Genetic tests Medical literature

Select item 6185225.

#618522 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59; MRD59

Cytogenetic locations: 30184290

OMIM:: 618522

Gene summaries Genetic tests Medical literature

Select item 6179916.

#617991 - CHUNG-JANSEN SYNDROME; CHUJANS

Cytogenetic locations: 27900362

OMIM:: 617991

Gene summaries Genetic tests Medical literature

Select item 6177967.

#617796 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 52; MRD52

Cytogenetic locations: 27824329

OMIM:: 617796

Gene summaries Genetic tests Medical literature

Select item 6173918.

#617391 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54; DEE54

Cytogenetic locations: 22581936

OMIM:: 617391

Gene summaries Genetic tests Medical literature

Select item 6165219.

#616521 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 39; MRD39

CHROMOSOME 2p25.3 DELETION SYNDROME, INCLUDED

Cytogenetic locations: 606416

OMIM:: 616521

Gene summaries Genetic tests Medical literature

Select item 61640910.

#616409 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33; DEE33

Cytogenetic locations: 603038

OMIM:: 616409

Gene summaries Genetic tests Medical literature

Select item 61536911.

#615369 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94

Cytogenetic locations: Stra6

OMIM:: 615369

Gene summaries Genetic tests Medical literature

Select item 61528212.

#615282 - CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 2; CDCBM2

Cytogenetic locations: 617878

OMIM:: 615282

Gene summaries Genetic tests Medical literature

Select item 61507513.

#615075 - NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV

Cytogenetic locations: 24614104

OMIM:: 615075

Gene summaries Genetic tests Medical literature

Select item 61507414.

#615074 - GAND SYNDROME; GAND

Cytogenetic locations: over-expressed

OMIM:: 615074

Gene summaries Genetic tests Medical literature

Select item 61504715.

*615047 - TETRATRICOPEPTIDE REPEAT-, ANKYRIN REPEAT-, AND COILED-COIL-CONTAINING PROTEIN 2; TANC2

Cytogenetic locations: 30021165

OMIM:: 615047

Gene summaries Genetic tests Medical literature

Select item 61499816.

*614998 - GATA ZINC FINGER DOMAIN-CONTAINING PROTEIN 2B; GATAD2B

Cytogenetic locations: over-expressed

OMIM:: 614998

Gene summaries Genetic tests Medical literature

Select item 61455817.

#614558 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 13; DEE13

Cytogenetic locations: 22365152

OMIM:: 614558

Gene summaries Genetic tests Medical literature

Select item 61372118.

#613721 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 11; DEE11

Cytogenetic locations: 28379373

OMIM:: 613721

Gene summaries Genetic tests Medical literature

Select item 61344319.

#613443 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL

CHROMOSOME 5q14.3 DELETION SYNDROME, PROXIMAL, INCLUDED

Cytogenetic locations: 20513142

OMIM:: 613443

Gene summaries Genetic tests Medical literature

Select item 61308420.

*613084 - MYELIN TRANSCRIPTION FACTOR 1-LIKE; MYT1L

Cytogenetic locations: 606416

OMIM:: 613084

Gene summaries Genetic tests Medical literature

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