Abnormality of the respiratory system
Symptom Information:
Symptom ID: | HPO:0002086 | ||||
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 respiratory system(HPO:0002086) MedDRA: |
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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) |