From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
Cytogenetic locations: 15q26.3
- OMIM:
- 608320
2.
Cytogenetic locations: 10p11.23
- OMIM:
- 614398
3.
Cytogenetic locations: 3q21.1-q21.2
- OMIM:
- 608901
4.
Cytogenetic locations: 19q13.2
- OMIM:
- 615812
5.
Cytogenetic locations: 12p13.2
- OMIM:
- 610947
6.
CORONARY ARTERY DISEASE, MODIFIER OF, INCLUDED
Cytogenetic locations: 17q12
- OMIM:
- 158105
7.
LIPOPROTEIN(a), INCLUDED; Lp(a), INCLUDED
Cytogenetic locations: 6q25-q26
- OMIM:
- 152200
8.
PON1 ENZYME ACTIVITY, VARIATION IN, INCLUDED
Cytogenetic locations: 7q21.3
- OMIM:
- 168820
9.
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO, INCLUDED
Cytogenetic locations: 13q13.1
- OMIM:
- 604824
10.
CORONARY ARTERY SPASM 1, SUSCEPTIBILITY TO, INCLUDED
Cytogenetic locations: 7q36.1
- OMIM:
- 163729
11.
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO, INCLUDED
Cytogenetic locations: 2q36.3
- OMIM:
- 147545
12.
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO, INCLUDED
Cytogenetic locations: 19q13.32
- OMIM:
- 617347
13.
Cytogenetic locations: 3p25.2
- OMIM:
- 609338
14.
Cytogenetic locations: 14q32
- OMIM:
- 608318
15.
Cytogenetic locations: 7q21.11
- OMIM:
- 610938
16.
Cytogenetic locations: 2q21.1-q22
- OMIM:
- 608316
17.
Cytogenetic locations: 1pter-p36.13, 16pter-p13
- OMIM:
- 607339
18.
CORONARY HEART DISEASE IN FAMILIAL HYPERCHOLESTEROLEMIA, PROTECTION AGAINST, INCLUDED
Cytogenetic locations: 9q31.1
- OMIM:
- 600046
19.
Cytogenetic locations: 9p21
- OMIM:
- 611139
20.
CORONARY SCLEROSIS, MEDIAL, OF INFANCY, INCLUDED
Cytogenetic locations: 6q23.2
- OMIM:
- 208000
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