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From NIH OMIM
OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.
Cytogenetic locations: 3p22.2
- OMIM:
- 120436
2.
Cytogenetic locations: Xq28
- OMIM:
- 300005
4.
Cytogenetic locations: 5p14.2
- OMIM:
- 609760
5.
Cytogenetic locations: 15q12
- OMIM:
- 137192
6.
FRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED
Cytogenetic locations: 9q21.11
- OMIM:
- 229300
7.
BECKWITH-WIEDEMANN SYNDROME CHROMOSOME REGION, INCLUDED; BWCR, INCLUDED
Cytogenetic locations: 1pter-p36.13, 11p15.5, 1pter-p36.13, 11p15.4
- OMIM:
- 130650
8.
Cytogenetic locations: 5q22.2
- OMIM:
- 611731
9.
Cytogenetic locations: 20q13.31
- OMIM:
- 607022
10.
Cytogenetic locations: 8p11.21
- OMIM:
- 604156
11.
Cytogenetic locations: 16q22.1
- OMIM:
- 604167
12.
Cytogenetic locations: 14q32.31
- OMIM:
- 140571
13.
Cytogenetic locations: 2q34
- OMIM:
- 147700
14.
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 13, INCLUDED; ALS13, INCLUDED
Cytogenetic locations: 12q24.12
- OMIM:
- 183090
15.
Cytogenetic locations: 19p13.2
- OMIM:
- 126375
16.
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO, 1, INCLUDED; MS1, INCLUDED
Cytogenetic locations: 6p21.32, 1pter-p36.13, 2q37.3
- OMIM:
- 126200
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