OMIM Links for Protein (Select 116242746) - OMIM - NCBI

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Links from Protein

Items: 1 to 20 of 42

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Select item 6199271.

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

Cytogenetic locations: 35675825

OMIM:: 619927

Gene summaries Genetic tests Medical literature

Select item 6196902.

#619690 - BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG

Cytogenetic locations: 33980986

OMIM:: 619690

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: 3'

OMIM:: 618906

Gene summaries Genetic tests Medical literature

Select item 6185224.

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

Cytogenetic locations: 30184290

OMIM:: 618522

Gene summaries Genetic tests Medical literature

Select item 6182985.

#618298 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70

Cytogenetic locations: 30256902

OMIM:: 618298

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 6165218.

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

CHROMOSOME 2p25.3 DELETION SYNDROME, INCLUDED

Cytogenetic locations: NLR

OMIM:: 616521

Gene summaries Genetic tests Medical literature

Select item 6164099.

#616409 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 33; DEE33

Cytogenetic locations: 23647072

OMIM:: 616409

Gene summaries Genetic tests Medical literature

Select item 61583510.

#615835 - CHROMOSOME 16 INVERSION, 0.45-MB

Cytogenetic locations: Thoc6

OMIM:: 615835

Gene summaries Genetic tests Medical literature

Select item 61528211.

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

Cytogenetic locations: 24812067

OMIM:: 615282

Gene summaries Genetic tests Medical literature

Select item 61507512.

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

Cytogenetic locations: 3p22.3

OMIM:: 615075

Gene summaries Genetic tests Medical literature

Select item 61507413.

#615074 - GAND SYNDROME; GAND

Cytogenetic locations: 23644463

OMIM:: 615074

Gene summaries Genetic tests Medical literature

Select item 61504714.

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

Cytogenetic locations: 3'

OMIM:: 615047

Gene summaries Genetic tests Medical literature

Select item 61499815.

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

Cytogenetic locations: 23644463

OMIM:: 614998

Gene summaries Genetic tests Medical literature

Select item 61484316.

*614843 - ODONTOGENIC AMELOBLAST-ASSOCIATED PROTEIN; ODAM

Cytogenetic locations: 14647039

OMIM:: 614843

Gene summaries Genetic tests Medical literature

Select item 61336717.

*613367 - LIN54, C. ELEGANS, HOMOLOG OF; LIN54

Cytogenetic locations: mutation

OMIM:: 613367

Gene summaries Genetic tests Medical literature

Select item 61308418.

*613084 - MYELIN TRANSCRIPTION FACTOR 1-LIKE; MYT1L

Cytogenetic locations: NLR

OMIM:: 613084

Gene summaries Genetic tests Medical literature

Select item 61287019.

*612870 - PLECKSTRIN HOMOLOGY DOMAIN-INTERACTING PROTEIN; PHIP

Cytogenetic locations: 27900362

OMIM:: 612870

Gene summaries Genetic tests Medical literature

Select item 61008920.

*610089 - RAD50-INTERACTING PROTEIN 1; RINT1

Cytogenetic locations: 11096100

OMIM:: 610089

Gene summaries Genetic tests Medical literature

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