Asthma

Symptom Information:

Symptom ID: HPO:0002099
Synonyms:
Bronchial asthma [HPO:0002099]
Reactive airway disease [HPO:0002099]
Asthma (disorder) [Orphanet:33300]
Asthma [Orphanet:33300]
Asthma [OMIM:Asthma]
Bronchial asthma [OMIM:Bronchial asthma]
Asthma/bronchospasm [Orphanet:33300]
Asthma [MedDRA:10003553]
Allergic asthma [MedDRA:10003553]
Asthma aggravated [MedDRA:10003553]
Asthma bronchial [MedDRA:10003553]
Asthma extrinsic [MedDRA:10003553]
Asthma NOS [MedDRA:10003553]
Asthma, unspecified [MedDRA:10003553]
Asthma, unspecified type, without mention of status asthmaticus [MedDRA:10003553]
Asthma/bronchitis [MedDRA:10003553]
Asthmatic [MedDRA:10003553]
Asthmatic attack [MedDRA:10003553]
Asthmatic attack induced [MedDRA:10003553]
Atopic asthma [MedDRA:10003553]
Br. asthma [MedDRA:10003553]
Bronchitic asthma [MedDRA:10003553]
Bronchitis asthmatic [MedDRA:10003553]
Chronic obstructive asthma (with obstructive pulmonary disease) [MedDRA:10003553]
Chronic obstructive asthma (with obstructive pulmonary disease), w/o-ment of status asthmaticus [MedDRA:10003553]
Chronic obstructive asthma (with obstructive pulmonary disease), w/o ment of status asthmaticus [MedDRA:10003553]
Exacerbation of asthma [MedDRA:10003553]
Extrinsic asthma [MedDRA:10003553]
Extrinsic asthma without mention of status asthmaticus [MedDRA:10003553]
Intrinsic asthma [MedDRA:10003553]
Intrinsic asthma without mention of status asthmaticus [MedDRA:10003553]
Asthma chronic [MedDRA:10003553]
Asthma-like condition [MedDRA:10003553]
Asthmatic attack atopic [MedDRA:10003553]
Drug-induced asthma [MedDRA:10003553]
Cough variant asthma [MedDRA:10003553]
Cold induced asthma [MedDRA:10003553]
Neutrophilic asthma [MedDRA:10003553]
Eosinophilic asthma [MedDRA:10003553]
Paucigranulocytic asthma [MedDRA:10003553]
Infection induced asthma [MedDRA:10003553]
Asthma (1 patient) [OMIM:Asthma (1 patient)]
Asthma (in some patients) [OMIM:Asthma (in some patients)]
Reactive airway disease [OMIM:Reactive airway disease]
Bronchospasm [MedDRA:10006482]
Bronchospasm (finding) [Orphanet:33300]
Bronchial Spasm [Orphanet:33300]
Bronchospasm [OMIM:Bronchospasm]
Quality:
Cross references:
Orphanet:33300 "Asthma/bronchospasm" [Orphanet:33300]
OMIM: "Asthma" [OMIM:Asthma]
OMIM: "Bronchial asthma" [OMIM:Bronchial asthma]
OMIM: "Asthma (1 patient)" [OMIM:Asthma (1 patient)]
OMIM: "Asthma (in some patients)" [OMIM:Asthma (in some patients)]
OMIM: "Reactive airway disease" [OMIM:Reactive airway disease]
OMIM: "Bronchospasm" [OMIM:Bronchospasm]
UMLS:C0004096 "Asthma" [HPO:0002099]
UMLS:C0004096 "Asthma" [Orphanet:33300]
UMLS:C0006266 "Bronchial Spasm" [Orphanet:33300]
Is a (Direct Parents):
HPO         Immunologic hypersensitivity
HPO         Abnormality of lung morphology
MedDRA Allergic conditions NEC
Orphanet Abnormality of the respiratory system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
             Immunologic hypersensitivity(HPO:0100326)
                Asthma(HPO:0002099)
       Abnormality of the respiratory system(HPO:0002086)
          Abnormal respiratory system morphology(HPO:0012252)
             Abnormality of lung morphology(HPO:0002088)
                Asthma(HPO:0002099)
MedDRA:
Immune system disorders(MedDRA:10021428)
    Allergic conditions(MedDRA:10001708)
       Allergic conditions NEC(MedDRA:10027654)
          Asthma(HPO:0002099)
Database Frequency: 62 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
48,XXXY syndrome (Orphanet:96263)
48,XXYY syndrome (Orphanet:10)
49,XXXXY syndrome (Orphanet:96264)
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY (OMIM:614262)
ASTHMA, NASAL POLYPS, AND ASPIRIN INTOLERANCE (OMIM:208550)
ASTHMA, SHORT STATURE, AND ELEVATED IgA (OMIM:208600)
ASTHMA, SUSCEPTIBILITY TO (OMIM:600807)
Aggressive systemic mastocytosis (Orphanet:98850)
Allergic bronchopulmonary aspergillosis (Orphanet:1164)
Alström syndrome (Orphanet:64)
Anisakiasis (Orphanet:1070)
Aortic arch defects (Orphanet:1132)
Autoimmune lymphoproliferative syndrome with recurrent infections (Orphanet:275517)
Autosomal recessive hyper-IgE syndrome (Orphanet:169446)
Bardet-Biedl syndrome (Orphanet:110)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 16 (OMIM:615993)
Bardet-Biedl syndrome 7 (OMIM:615984)
Brain-lung-thyroid syndrome (Orphanet:209905)
CILIARY DYSKINESIA, PRIMARY, 30 (OMIM:616037)
Combined immunodeficiency due to DOCK8 deficiency (Orphanet:217390)
Congenital ichthyosis - intellectual deficit - spastic quadriplegia (Orphanet:352333)
Cutaneous mastocytosis (Orphanet:66646)
Cystic fibrosis (Orphanet:586)
DERMATITIS, ATOPIC (OMIM:603165)
Dubowitz syndrome (Orphanet:235)
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME (OMIM:616029)
EHLERS-DANLOS SYNDROME, AUTOSOMAL DOMINANT, TYPE UNSPECIFIED (OMIM:130090)
Ehlers-Danlos syndrome, classic type (Orphanet:287)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Generalized peeling skin syndrome (Orphanet:263543)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
ICHTHYOSIS VULGARIS (OMIM:146700)
IMMUNODEFICIENCY 23 (OMIM:615816)
IMMUNODEFICIENCY, COMMON VARIABLE, 10 (OMIM:615577)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
IgE RESPONSIVENESS, ATOPIC (OMIM:147050)
Isobutyryl-CoA dehydrogenase deficiency (Orphanet:79159)
Keratosis pilaris atrophicans (Orphanet:498)
Mastocytosis (Orphanet:98292)
Monosomy 18q (Orphanet:1600)
Mucopolysaccharidosis type 2 (Orphanet:580)
Myotonia permanens (Orphanet:99735)
Netherton syndrome (Orphanet:634)
PLCG2-associated antibody deficiency and immune dysregulation (Orphanet:300359)
Pancreatic insufficiency - anemia - hyperostosis (Orphanet:199337)
Peeling skin syndrome type B (Orphanet:263553)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Prolidase deficiency (Orphanet:742)
Roifman syndrome (Orphanet:353298)
Scheie syndrome (Orphanet:93474)
Severe combined immunodeficiency due to adenosine deaminase deficiency (Orphanet:277)
Solitary median maxillary central incisor syndrome (Orphanet:2286)
Stüve-Wiedemann syndrome (Orphanet:3206)
Sudden infant death - dysgenesis of the testes (Orphanet:168593)
Systemic mastocytosis (Orphanet:2467)
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE (OMIM:601675)