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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.
VARIEGATE PORPHYRIA, HOMOZYGOUS VARIANT, INCLUDED
Cytogenetic locations: 1pter-p36.13, 1q23.3
- OMIM:
- 176200
2.
Cytogenetic locations: 1q21.2
- OMIM:
- 247100
3.
SCHIZOPHRENIA 17, INCLUDED; SCZD17, INCLUDED
Cytogenetic locations: 2p16.3
- OMIM:
- 614332
4.
Cytogenetic locations: Xp11.3
- OMIM:
- 309860
5.
Cytogenetic locations: 2p16.3
- OMIM:
- 600565
6.
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY, INCLUDED
Cytogenetic locations: 5q31.3, 1pter-p36.13, 5q11.2, 1pter-p36.13, 5p15.33, 1pter-p36.13, 2q37.3, 1pter-p36.13, 2q35, 1pter-p36.13, 19p13.3, 1pter-p36.13, 17p12, 1pter-p36.13, 12q22
- OMIM:
- 256000
7.
Cytogenetic locations: 22q11.21
- OMIM:
- 192430
8.
ALZHEIMER DISEASE, FAMILIAL, 1, INCLUDED; AD1, INCLUDED
Cytogenetic locations: 1pter-p36.13, 6p22.2, 1pter-p36.13, 21q21.3, 1pter-p36.13, 17q22
- OMIM:
- 104300
9.
Cytogenetic locations: 1pter-p36.13, 22q12.3, 1pter-p36.13, 22q11.21, 1pter-p36.13, 22q11.21, 1pter-p36.13, 1q32.1, 1pter-p36.13, 18p, 1pter-p36.13, 1p36.2, 1pter-p36.13, 14q32.33, 1pter-p36.13, 13q33.2, 1pter-p36.13, 13q32, 1pter-p36.13, 13q14.1pter-p36.13, 22q12.3, 1pter-p36.13, 22q11.21, 1pter-p36.13, 22q11.21, 1pter-p36.13, 1q32.1, 1pter-p36.13, 18p, 1pter-p36.13, 1p36.2, 1pter-p36.13, 14q32.33, 1pter-p36.13, 13q33.2, 1pter-p36.13, 13q32, 1pter-p36.13, 13q1
- OMIM:
- 181500
10.
AUTISM, SUSCEPTIBILITY TO, 1, INCLUDED; AUTS1, INCLUDED
Cytogenetic locations: 7q22
- OMIM:
- 209850
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