From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
COUMARIN SENSITIVITY, INCLUDED
Cytogenetic locations: 1pter-p36.13, 19q13.2, 1pter-p36.13, 16p11.2
- OMIM:
- 122700
2.
CHONDRODYSPLASIA PUNCTATA DUE TO VITAMIN K DEFICIENCY, INCLUDED
- OMIM:
- 118650
3.
Cytogenetic locations: 16p11.2
- OMIM:
- 608547
4.
Cytogenetic locations: 10q23.33
- OMIM:
- 601130
5.
PROTEIN C DEFICIENCY, ACQUIRED, INCLUDED
Cytogenetic locations: 2q14.3
- OMIM:
- 176860
6.
Cytogenetic locations: Xq27.1
- OMIM:
- 300746
7.
Cytogenetic locations: 3q11.1
- OMIM:
- 612336
8.
FACTOR V LEIDEN, INCLUDED
Cytogenetic locations: 1q24.2
- OMIM:
- 612309
9.
Cytogenetic locations: 7q11.21
- OMIM:
- 608838
10.
Cytogenetic locations: 2p11.2
- OMIM:
- 277450
11.
Cytogenetic locations: Xp22.33
- OMIM:
- 300003
12.
Cytogenetic locations: 19p13.12
- OMIM:
- 604426
13.
Cytogenetic locations: 16p11.2
- OMIM:
- 607473
14.
Cytogenetic locations: Xp22.33
- OMIM:
- 300180
15.
Cytogenetic locations: 2q14.3
- OMIM:
- 612304
16.
Cytogenetic locations: Xp22.33
- OMIM:
- 302950
17.
18.
Cytogenetic locations: 12p12.3
- OMIM:
- 245150
19.
Cytogenetic locations: 15q15.1
- OMIM:
- 600341
20.
Cytogenetic locations: 19q13.2
- OMIM:
- 109135
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