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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.
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, MITOCHONDRIAL TYPE 1, INCLUDED; MC5DM1, INCLUDED
- OMIM:
- 516060
2.
Cytogenetic locations: 12q13.12
- OMIM:
- 601906
3.
Cytogenetic locations: 21q22.3
- OMIM:
- 120240
4.
Cytogenetic locations: 7q34
- OMIM:
- 118425
5.
Cytogenetic locations: 13q12.11
- OMIM:
- 121011
6.
Cytogenetic locations: 7q31.2
- OMIM:
- 602421
7.
Cytogenetic locations: 14q22.1
- OMIM:
- 182600
8.
Cytogenetic locations: 1q25.2
- OMIM:
- 604766
9.
Cytogenetic locations: 19q13.32
- OMIM:
- 160900
10.
Cytogenetic locations: 5q32
- OMIM:
- 226900
11.
RETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED
Cytogenetic locations: 11q14.2
- OMIM:
- 133780
12.
13.
Cytogenetic locations: 1pter-p36.13, 2q36.3
- OMIM:
- 203780
14.
CEREBRAL CAVERNOUS MALFORMATIONS 1, INCLUDED; CCM1, INCLUDED
Cytogenetic locations: 7q21.2
- OMIM:
- 116860
15.
Cytogenetic locations: 17p12
- OMIM:
- 118220
16.
FRIEDREICH ATAXIA WITH RETAINED REFLEXES, INCLUDED; FARR, INCLUDED
Cytogenetic locations: 9q21.11
- OMIM:
- 229300
17.
Cytogenetic locations: 3p24.1
- OMIM:
- 610168
18.
Cytogenetic locations: 9q34.11
- OMIM:
- 187300
19.
Cytogenetic locations: 11p15.1
- OMIM:
- 256450
20.
Cytogenetic locations: 9q34.13
- OMIM:
- 191100
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