From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
LEANNESS, INCLUDED
Cytogenetic locations: 5q13.2, 1pter-p36.13, 4q31.1, 1pter-p36.13, 3p25.2, 1pter-p36.13, 3p25.3, 1pter-p36.13, 1p36.11, 1pter-p36.13, 2p23.3, 1pter-p36.13, 18q21.32, 1pter-p36.13, 16q22.1
- OMIM:
- 601665
2.
Cytogenetic locations: 1p36.11
- OMIM:
- 607404
3.
#226300 - COMPLEMENT HYPERACTIVATION, ANGIOPATHIC THROMBOSIS, AND PROTEIN-LOSING ENTEROPATHY; CHAPLE
Cytogenetic locations: 1q32.2
- OMIM:
- 226300
4.
Cytogenetic locations: Xp22.2
- OMIM:
- 300335
5.
Cytogenetic locations: 2q37.1
- OMIM:
- 610767
6.
Cytogenetic locations: 16q12.1
- OMIM:
- 605956
7.
Cytogenetic locations: 2p22.3
- OMIM:
- 606831
8.
Cytogenetic locations: 3p22.2
- OMIM:
- 602170
9.
Cytogenetic locations: 12q23.2
- OMIM:
- 147440
10.
Cytogenetic locations: 4q31.3
- OMIM:
- 603028
11.
Cytogenetic locations: 9q33.1
- OMIM:
- 603030
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