OMIM Links for GEO Profiles (Select 3642852) - OMIM

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Links from GEO Profiles

Items: 8

Select item 6181841.

#618184 - NEUROPATHY, CONGENITAL HYPOMYELINATING, 2; CHN2

Cytogenetic locations: 18816708

OMIM:: 618184

Gene summaries Genetic tests Medical literature

Select item 6077912.

#607791 - CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE D; CMTDID

Cytogenetic locations: 10406984

OMIM:: 607791

Gene summaries Genetic tests Medical literature

Select item 6077363.

#607736 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2J; CMT2J

OMIM:: 607736

Gene summaries Genetic tests Medical literature

Select item 6076774.

#607677 - CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2I; CMT2I

Cytogenetic locations: 10764043

OMIM:: 607677

Gene summaries Genetic tests Medical literature

Select item 1808005.

#180800 - ROUSSY-LEVY HEREDITARY AREFLEXIC DYSTASIA

Cytogenetic locations: 1p36, 1p36

OMIM:: 180800

Gene summaries Genetic tests Medical literature

Select item 1594406.

*159440 - MYELIN PROTEIN ZERO; MPZ

Cytogenetic locations: 11709914

OMIM:: 159440

Gene summaries Genetic tests Medical literature

Select item 1459007.

#145900 - HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS

Cytogenetic locations: 1p36, 1p36, 1p36

OMIM:: 145900

Gene summaries Genetic tests Medical literature

Select item 1182008.

#118200 - CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B

Cytogenetic locations: 15027400

OMIM:: 118200

Gene summaries Genetic tests Medical literature

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