sábado, 28 de julio de 2018

Chronic obstructive pulmonary disease - OMIM - NCBI

Chronic obstructive pulmonary disease - OMIM - NCBI

x ray of a lung

From NIH OMIM

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







PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, SEVERE EARLY-ONSET, INCLUDED
Cytogenetic locations: 1pter-p36.13, 22q12.3, 1pter-p36.13, 14q32.13
3.
FABRY DISEASE, CARDIAC VARIANT, INCLUDED
Cytogenetic locations: Xq22.1
5.
8.
9.
11.
12.
13.
Cytogenetic locations: 19q13.2, 1pter-p36.13, 1q23.3
15.
16.
PTERYGIUM COLLI SYNDROME, INCLUDED
Cytogenetic locations: 12q24.13
17.
18.
MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES, INCLUDED; CMEMS, INCLUDED
Cytogenetic locations: 11p15.5
19.

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