Neonatal respiratory distress

Symptom Information:

Symptom ID: HPO:0002643
Synonyms:
Infantile respiratory distress [HPO:0002643]
Newborn respiratory distress [HPO:0002643]
Respiratory distress, neonatal [HPO:0002643]
Infantile respiratory distress [OMIM:Infantile respiratory distress]
Neonatal respiratory distress [OMIM:Neonatal respiratory distress]
Newborn respiratory distress [OMIM:Newborn respiratory distress]
Respiratory distress, neonatal [OMIM:Respiratory distress, neonatal]
Quality:
Cross references:
OMIM: "Infantile respiratory distress" [OMIM:Infantile respiratory distress]
OMIM: "Neonatal respiratory distress" [OMIM:Neonatal respiratory distress]
OMIM: "Newborn respiratory distress" [OMIM:Newborn respiratory distress]
OMIM: "Respiratory distress, neonatal" [OMIM:Respiratory distress, neonatal]
Is a (Direct Parents):
HPO         Neonatal asphyxia
HPO         Respiratory insufficiency
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
          Functional respiratory abnormality(HPO:0002795)
             Respiratory insufficiency(HPO:0002093)
                Neonatal respiratory distress(HPO:0002643)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Respiratory insufficiency(HPO:0002093)
                   Neonatal respiratory distress(HPO:0002643)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 4 (Orphanet:67048)
3M syndrome (Orphanet:2616)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Brain-lung-thyroid syndrome (Orphanet:209905)
Cerebro-costo-mandibular syndrome (Orphanet:1393)
Cleidocranial dysplasia (Orphanet:1452)
Congenital nephrotic syndrome, Finnish type (Orphanet:839)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Fetal Gaucher disease (Orphanet:85212)
Hyper-beta-alaninemia (Orphanet:309147)
Infant acute respiratory distress syndrome (Orphanet:70587)
Intellectual disability-developmental delay-contractures syndrome (Orphanet:3454)
Isolated Pierre Robin syndrome (Orphanet:718)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
Pyridoxine-dependent epilepsy (Orphanet:3006)
Shwachman-Diamond syndrome (Orphanet:811)
Steinert myotonic dystrophy (Orphanet:273)
THORACOPELVIC DYSOSTOSIS (OMIM:187770)
THREE M SYNDROME 1 (OMIM:273750)
X-linked centronuclear myopathy (Orphanet:596)