DiseaseID 5059
肺透明膜病
disease
MSH2017_2016_08_12:A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining th
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 12Target: 12Links: 24
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5059
- Core Entity Id
- 61500
- Source Entity Count
- 1
- Preferred Name
- Hyaline Membrane Disease
- Name Cn
- 肺透明膜病
- Name Pinyin
- Fei Tou Ming Mo Bing
- Name En
- Hyaline Membrane Disease
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS).
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hyaline Membrane Disease
Role
preferred
Name
Respiratory Distress Syndrome, Newborn
Role
preferred
Name
Newborn Respiratory Distress Syndrome
Role
alias
Name
Respiratory Distress Syndrome of Newborn
Role
alias
Name
Respiratory Distress of Newborn
Role
alias
Name
Respiratory Distress of Newborn, Unspecified
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS001405HBDIS002595
Me Sh
D006819D012127
Umls
C0020192C0035220
Icd10
P22P22.0P22.9
Sym Map
SMDE09560SMDE12815
Do Class
DOID:7
Dis Ge Net
C0020192C0035220
Umls Sty
T047
Me Sh Class
C08C16
Tcmbank Disease
106827107
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Disease Definition
MSH2017_2016_08_12:A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS).NCI2016_NICHD_1602D:Progressive alveolar atelectasis from birth due to an abnormality of synthesis, function or metabolism of surfactant, characterized by respiratory failure and an abnormal chest radiograph showing diffuse reticulogranular densities and air bronchograms.|NCI2016_FDA_1602D:A condition of the newborn marked by dyspnea with cyanosis, most frequently occurring in premature infants, children of diabetic mothers and infants delivered by cesarean section, and sometimes with no predisposing cause.|NCI2016_02D:A condition beginning in the first day of life that results from inadequate surfactant production, causing increased work of breathing and impaired gas exchange.(NICHD)|MSH2017_2016_08_12:A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause.|CSP2006:a condition of the newborn marked by dyspnea with cyanosis, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, most frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
Umls Semantic Type Name
Disease or Syndrome