Chronic obstructive pulmonary disease - OMIM - NCBI

Chronic obstructive pulmonary disease - 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 "Chronic obstructive pulmonary disease" 

%606963 - PULMONARY DISEASE, CHRONIC OBSTRUCTIVE; COPD

PULMONARY DISEASE, CHRONIC OBSTRUCTIVE, SEVERE EARLY-ONSET, INCLUDED

Cytogenetic locations: 1pter-p36.13, 22q12.3, 1pter-p36.13, 14q32.13

OMIM:

 

606963

Gene summaries Genetic tests Medical literature

Select item 1307002.

130700 - EMPHYSEMA, HEREDITARY PULMONARY

OMIM:

 

130700

Gene summaries Genetic tests Medical literature

Select item 3015003.

#301500 - FABRY DISEASE

FABRY DISEASE, CARDIAC VARIANT, INCLUDED

Cytogenetic locations: Xq22.1

OMIM:

 

301500

Gene summaries Genetic tests Medical literature

Select item 2426804.

242680 - CILIARY DYSKINESIA WITH EXCESSIVELY LONG CILIA

OMIM:

 

242680

Gene summaries Genetic tests Medical literature

Select item 1412505.

*141250 - HEME OXYGENASE 1; HMOX1

Cytogenetic locations: 22q12.3

OMIM:

 

141250

Gene summaries Genetic tests Medical literature

Select item 1074006.

*107400 - SERPIN PEPTIDASE INHIBITOR, CLADE A, MEMBER 1; SERPINA1

Cytogenetic locations: 14q32.13

OMIM:

 

107400

Gene summaries Genetic tests Medical literature

Select item 6165767.

#616576 - IMMUNODEFICIENCY, COMMON VARIABLE, 12; CVID12

Cytogenetic locations: 4q24

OMIM:

 

616576

Gene summaries Genetic tests Medical literature

Select item 6134908.

#613490 - ALPHA-1-ANTITRYPSIN DEFICIENCY; A1ATD

Cytogenetic locations: 14q32.13

OMIM:

 

613490

Gene summaries Genetic tests Medical literature

Select item 2451509.

#245150 - KEUTEL SYNDROME; KTLS

Cytogenetic locations: 12p12.3

OMIM:

 

245150

Gene summaries Genetic tests Medical literature

Select item 61272610.

%612726 - HARDIKAR SYNDROME

OMIM:

 

612726

Gene summaries Genetic tests Medical literature

Select item 61548211.

#615482 - CILIARY DYSKINESIA, PRIMARY, 25; CILD25

Cytogenetic locations: 15q21.3

OMIM:

 

615482

Gene summaries Genetic tests Medical literature

Select item 60480912.

%604809 - PANBRONCHIOLITIS, DIFFUSE

Cytogenetic locations: 6p21.3

OMIM:

 

604809

Gene summaries Genetic tests Medical literature

Select item 21970013.

#219700 - CYSTIC FIBROSIS; CF

Cytogenetic locations: 19q13.2, 1pter-p36.13, 1q23.3

OMIM:

 

219700

Gene summaries Genetic tests Medical literature

Select item 60077014.

*600770 - MUCIN 5, SUBTYPE B, TRACHEOBRONCHIAL; MUC5B

Cytogenetic locations: 11p15.5

OMIM:

 

600770

Gene summaries Genetic tests Medical literature

Select item 19405015.

#194050 - WILLIAMS-BEUREN SYNDROME; WBS

Cytogenetic locations: 7q11.23

OMIM:

 

194050

Gene summaries Genetic tests Medical literature

Select item 16395016.

#163950 - NOONAN SYNDROME 1; NS1

PTERYGIUM COLLI SYNDROME, INCLUDED

Cytogenetic locations: 12q24.13

OMIM:

 

163950

Gene summaries Genetic tests Medical literature

Select item 15110017.

#151100 - LEOPARD SYNDROME 1; LPRD1

Cytogenetic locations: 12q24.13

OMIM:

 

151100

Gene summaries Genetic tests Medical literature

Select item 21804018.

#218040 - COSTELLO SYNDROME; CSTLO

MYOPATHY, CONGENITAL, WITH EXCESS OF MUSCLE SPINDLES, INCLUDED; CMEMS, INCLUDED

Cytogenetic locations: 11p15.5

OMIM:

 

218040

Gene summaries Genetic tests Medical literature

Select item 61780319.

*617803 - TRANSMEMBRANE PROTEIN 26; TMEM26

Cytogenetic locations: 10q21.2

OMIM:

 

617803

Gene summaries Genetic tests Medical literature

Select item 10728020.

*107280 - SERPIN PEPTIDASE INHIBITOR, CLADE A, MEMBER 3; SERPINA3

Cytogenetic locations: 14q32.13

OMIM:

 

107280

Gene summaries Genetic tests Medical literature