lunes, 2 de julio de 2018

Adrenoleukodystrophy - OMIM - NCBI

Adrenoleukodystrophy - OMIM - NCBI

a brain

From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.



5.
ADRENOMYELONEUROPATHY, INCLUDED; AMN, INCLUDED
Cytogenetic locations: Xq28
6.
7.
9.
11.
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 1, INCLUDED; CG1, INCLUDED
Cytogenetic locations: 7q21.2
14.
20.
CONTIGUOUS ABCD1/DXS1375E DELETION SYNDROME, INCLUDED; CADDS, INCLUDED
Cytogenetic locations: Xq28

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