Respiratory difficulties
Symptom Information:
Symptom ID: | HPO:0002880 | ||
Synonyms: |
|
||
Quality: | |||
Cross references: |
|
||
Is a (Direct Parents): |
|
||
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) |