From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
2.
MECONIUM ILEUS IN CYSTIC FIBROSIS, SUSCEPTIBILITY TO, INCLUDED
Cytogenetic locations: 19q13.2-q13.4
- OMIM:
- 603855
3.
Cytogenetic locations: 16p12.2
- OMIM:
- 613071
4.
Cytogenetic locations: 12p13.31
- OMIM:
- 613021
5.
Cytogenetic locations: 1pter-p36.13, 16p12.2
- OMIM:
- 211400
6.
Cytogenetic locations: 7q31.2
- OMIM:
- 602421
7.
Cytogenetic locations: 19q13.2, 1pter-p36.13, 1q23.3
- OMIM:
- 219700
8.
S100A9/S100A8 COMPLEX, INCLUDED
Cytogenetic locations: 1q21.3
- OMIM:
- 123886
9.
S100A8/S100A9 COMPLEX, INCLUDED
Cytogenetic locations: 1q21.3
- OMIM:
- 123885
10.
11.
Cytogenetic locations: 1q22
- OMIM:
- 174000
12.
Cytogenetic locations: 4p15.32, 1pter-p36.13, 16q12.2
- OMIM:
- 216360
13.
HEPATIC FIBROSIS, CONGENITAL, INCLUDED
Cytogenetic locations: 6p12.3-p12.2
- OMIM:
- 263200
14.
HAMMAN-RICH DISEASE, INCLUDED
Cytogenetic locations: 1pter-p36.13, 10q22.3
- OMIM:
- 178500
15.
Cytogenetic locations: 7q31.2
- OMIM:
- 277180
16.
17.
Cytogenetic locations: 19q13.2
- OMIM:
- 190180
18.
Cytogenetic locations: 17q11.2
- OMIM:
- 615415
19.
Cytogenetic locations: 15q13
- OMIM:
- 208500
20.
Cytogenetic locations: 12p12.3
- OMIM:
- 614665
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