Format
Items per page

Send to:

Choose Destination

Links from PubMed

Items: 14

1.

Respiratory failure

A severe form of respiratory insufficiency characterized by inadequate gas exchange such that the levels of oxygen or carbon dioxide cannot be maintained within normal limits. [from HPO]

MedGen UID:
257837
Concept ID:
C1145670
Disease or Syndrome
2.

Newborn

MedGen UID:
745693
Concept ID:
C2239178
Finding
3.

Furriers lung

MedGen UID:
538594
Concept ID:
C0264476
Disease or Syndrome
4.

Coffee-workers lung

MedGen UID:
538589
Concept ID:
C0264468
Disease or Syndrome
5.

Cheese-washers lung

MedGen UID:
507549
Concept ID:
C0007969
Disease or Syndrome
6.

Respiratory system agent

Drugs used for their effects on the respiratory system. [from MeSH]

MedGen UID:
76498
Concept ID:
C0282686
Pharmacologic Substance
7.

Disorder of respiratory system

A non-neoplastic or neoplastic disorder that affects the respiratory system. Representative examples include pneumonia, chronic obstructive pulmonary disease, pulmonary failure, lung adenoma, lung carcinoma, and tracheal carcinoma. [from NCI]

MedGen UID:
48421
Concept ID:
C0035204
Disease or Syndrome
8.

Diseases, Respiratory Tract

Diseases involving the RESPIRATORY SYSTEM. [from MeSH]

MedGen UID:
19750
Concept ID:
C0035242
Disease or Syndrome
9.

Respiratory surfactant

Pulmonary surfactant lines the lung epithelium and lowers surface tension to prevent collapse at end-expiration. Deficiency of pulmonary surfactant results in respiratory distress syndrome (RDS) in premature infants. Lung surfactant is synthesized in alveolar type II cells, stored in lamellar bodies and secreted via exocytosis. [from NCI]

MedGen UID:
18766
Concept ID:
C0034085
Biologically Active Substance; Organic Chemical; Pharmacologic Substance
10.

Respiratory insufficiency

Failure to adequately provide oxygen to cells of the body and to remove excess carbon dioxide from them. (Stedman, 25th ed) [from MeSH]

MedGen UID:
11197
Concept ID:
C0035229
Pathologic Function
11.

Bilateral complete cleft lip and/or alveolus

MedGen UID:
609340
Concept ID:
C0432088
Congenital Abnormality
12.

Unilateral complete cleft lip and/or alveolus

MedGen UID:
609338
Concept ID:
C0432086
Congenital Abnormality
13.

Unilateral incomplete cleft lip and/or alveolus

MedGen UID:
609337
Concept ID:
C0432085
Congenital Abnormality
14.

Surfactant metabolism dysfunction, pulmonary, 5

Pulmonary surfactant metabolism dysfunction-5 (SMDP5) is an autosomal recessive lung disorder manifest clinically and pathologically as pulmonary alveolar proteinosis (PAP). PAP is a rare lung disease characterized by the ineffective clearance of surfactant by alveolar macrophages. This results in the accumulation of surfactant-derived lipoproteinaceous material in the alveoli and terminal bronchioles, causing respiratory failure (summary by Greenhill and Kotton, 2009). For a general phenotypic description and a discussion of genetic heterogeneity of pulmonary surfactant metabolism dysfunction, see SMDP1 (265120). [from GTR]

MedGen UID:
482204
Concept ID:
C3280574
Disease or Syndrome
Format
Items per page

Send to:

Choose Destination

Supplemental Content

Find related data

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
Support Center