Asthma
Symptom Information:
Symptom ID: | HPO:0002099 | ||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |