Respiratory difficulties

Symptom Information:

Symptom ID: HPO:0002880
Synonyms:
Respiratory difficulties [OMIM:Respiratory difficulties]
Quality:
Cross references:
OMIM: "Respiratory difficulties" [OMIM:Respiratory difficulties]
Is a (Direct Parents):
HPO         Functional respiratory abnormality
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 difficulties(HPO:0002880)
MedDRA:
Database Frequency: 15 / 7739
Resource:

All diseases associated with this symptom:

CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 1 (OMIM:604377)
DIAMOND-BLACKFAN ANEMIA 10 (OMIM:613309)
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 30 (OMIM:616341)
Fatal infantile cytochrome C oxidase deficiency (Orphanet:1561)
Isolated congenital hypoglossia/aglossia (Orphanet:141152)
Isolated cytochrome C oxidase deficiency (Orphanet:254905)
Laron syndrome with immunodeficiency (Orphanet:220465)
Leigh syndrome (Orphanet:506)
Mandibulofacial dysostosis-microcephaly syndrome (Orphanet:79113)
Moebius syndrome (Orphanet:570)
Mucopolysaccharidosis type 2 (Orphanet:580)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
STT3B-CDG (Orphanet:370924)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
[DEL] LEIGH SYNDROME, X-LINKED (OMIM:308930)