Abnormality of the respiratory system

Symptom Information:

Symptom ID: HPO:0002086
Synonyms:
Respiratory abnormality [HPO:0002086]
Respiratory tract functional anomaly [Orphanet:33000]
Functional anomalies of the respiratory system and diaphragm [Orphanet:33000]
Diaphragm functional anomaly [Orphanet:33000]
Quality:
Cross references:
Orphanet:33000 "Functional anomalies of the respiratory system and diaphragm" [Orphanet:33000]
Is a (Direct Parents):
HPO         Phenotypic abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the respiratory system(HPO:0002086)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Autosomal dominant Charcot-Marie-Tooth disease type 2J (Orphanet:99943)
Blue rubber bleb nevus (Orphanet:1059)
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME (OMIM:215250)
Chronic hiccup (Orphanet:396)
Encephalopathy due to hydroxykynureninuria (Orphanet:79155)
FASCIAL DYSTROPHY, CONGENITAL (OMIM:228020)
HEMOSIDEROSIS, PULMONARY, WITH DEFICIENCY OF GAMMA-A GLOBULIN (OMIM:235500)
Heterotaxia (Orphanet:450)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hurler syndrome (Orphanet:93473)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Microcephaly - cardiac defect - lung malsegmentation (Orphanet:2516)
Pulmonary nodular lymphoid hyperplasia (Orphanet:60026)
RHEUMATOID ARTHRITIS (OMIM:180300)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Tuberous sclerosis (Orphanet:805)