OMIM Links for Gene (Select 3098) - OMIM - NCBI

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Links from Gene

Items: 5

Select item 6185471.

#618547 - NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES; NEDVIBA

Cytogenetic locations: 30778173

OMIM:: 618547

Gene summaries Genetic tests Medical literature

Select item 6174602.

#617460 - RETINITIS PIGMENTOSA 79; RP79

Cytogenetic locations: 25316723

OMIM:: 617460

Gene summaries Genetic tests Medical literature

Select item 6052853.

#605285 - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE; HMSNR

Cytogenetic locations: 11601496

OMIM:: 605285

Gene summaries Genetic tests Medical literature

Select item 2357004.

#235700 - ANEMIA, CONGENITAL, NONSPHEROCYTIC HEMOLYTIC, 5; CNSHA5

Cytogenetic locations: 12393545

OMIM:: 235700

Gene summaries Genetic tests Medical literature

Select item 1426005.

*142600 - HEXOKINASE 1; HK1

Cytogenetic locations: 25316723

OMIM:: 142600

Gene summaries Genetic tests Medical literature

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OMIM Links for Gene (Select 3098) (5)
OMIM
hexokinase-1 isoform HKI-R [Homo sapiens]
hexokinase-1 isoform HKI-R [Homo sapiens]
gi|15991827|ref|NP_277031.1|

Protein

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