Osteoporosis - OMIM - NCBI

Osteoporosis - OMIM - NCBI



From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.

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• Search OMIM for "Osteoporosis" 

204730 - AMINO ACIDURIA WITH MENTAL DEFICIENCY, DWARFISM, MUSCULAR DYSTROPHY, OSTEOPOROSIS, AND ACIDOSIS

OMIM:

 

204730

Gene summaries Genetic tests Medical literature

Select item 2597502.

259750 - OSTEOPOROSIS, JUVENILE

OMIM:

 

259750

Gene summaries Genetic tests Medical literature

Select item 6012203.

601220 - OSTEOPOROSIS AND OCULOCUTANEOUS HYPOPIGMENTATION SYNDROME; OOCH

OMIM:

 

601220

Gene summaries Genetic tests Medical literature

Select item 2480104.

248010 - MACROEPIPHYSEAL DYSPLASIA WITH OSTEOPOROSIS, WRINKLED SKIN, AND AGED APPEARANCE

OMIM:

 

248010

Gene summaries Genetic tests Medical literature

Select item 6082785.

608278 - GROWTH FAILURE, MICROCEPHALY, MENTAL RETARDATION, CATARACTS, LARGE JOINT CONTRACTURES, OSTEOPOROSIS, CORTICAL DYSPLASIA, AND CEREBELLAR ATROPHY

OMIM:

 

608278

Gene summaries Genetic tests Medical literature

Select item 6117396.

%611739 - BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 8; BMND8

Cytogenetic locations: 11p12

OMIM:

 

611739

Gene summaries Genetic tests Medical literature

Select item 6134187.

#613418 - BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15; BMND15

Cytogenetic locations: 9q34.11

OMIM:

 

613418

Gene summaries Genetic tests Medical literature

Select item 3009108.

#300910 - BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 18; BMND18

Cytogenetic locations: Xq23

OMIM:

 

300910

Gene summaries Genetic tests Medical literature

Select item 6122879.

#612287 - NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 2; NPHLOP2

Cytogenetic locations: 17q25.1

OMIM:

 

612287

Gene summaries Genetic tests Medical literature

Select item 61228610.

#612286 - NEPHROLITHIASIS/OSTEOPOROSIS, HYPOPHOSPHATEMIC, 1; NPHLOP1

Cytogenetic locations: 5q35.3

OMIM:

 

612286

Gene summaries Genetic tests Medical literature

Select item 61522111.

#615221 - BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 16; BMND16

Cytogenetic locations: 12q13.12

OMIM:

 

615221

Gene summaries Genetic tests Medical literature

Select item 25977012.

#259770 - OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG

Cytogenetic locations: 11q13.2

OMIM:

 

259770

Gene summaries Genetic tests Medical literature

Select item 16671013.

#166710 - OSTEOPOROSIS

FRACTURE, HIP, SUSCEPTIBILITY TO, INCLUDED

Cytogenetic locations: 1pter-p36.13, 7q21.3, 1pter-p36.13, 5q31.1, 1pter-p36.13, 20p12.3, 1pter-p36.13, 17q21.33

OMIM:

 

166710

Gene summaries Genetic tests Medical literature

Select item 60188414.

#601884 - BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1; BMND1

HIGH BONE MASS, INCLUDED; HBM, INCLUDED

Cytogenetic locations: 11q13.2

OMIM:

 

601884

Gene summaries Genetic tests Medical literature

Select item 10250015.

#102500 - HAJDU-CHENEY SYNDROME; HJCYS

Cytogenetic locations: 1p12

OMIM:

 

102500

Gene summaries Genetic tests Medical literature

Select item 60181116.

601811 - PREMATURE AGING SYNDROME, OKAMOTO TYPE

OMIM:

 

601811

Gene summaries Genetic tests Medical literature

Select item 26401017.

264010 - PRADER-WILLI HABITUS, OSTEOPENIA, AND CAMPTODACTYLY

OMIM:

 

264010

Gene summaries Genetic tests Medical literature

Select item 25672018.

256720 - NEUROLOGIC DISEASE, INFANTILE MULTISYSTEM, WITH OSSEOUS FRAGILITY

OMIM:

 

256720

Gene summaries Genetic tests Medical literature

Select item 16623019.

166230 - OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIAN BONES, BUT WITHOUT FRACTURES

OMIM:

 

166230

Gene summaries Genetic tests Medical literature

Select item 60350620.

*603506 - LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED PROTEIN 5; LRP5

Cytogenetic locations: 11q13.2

OMIM:

 

603506

Gene summaries Genetic tests Medical literature