Recurrent upper respiratory tract infections
Symptom Information:
Symptom ID: | HPO:0002788 | |||||||||||||||
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 head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the pharynx(HPO:0000600) Abnormality of the nasopharynx(HPO:0001739) Recurrent upper respiratory tract infections(HPO:0002788) Abnormality of the face(HPO:0000271) Abnormality of the nose(HPO:0000366) Abnormality of the nasopharynx(HPO:0001739) Recurrent upper respiratory tract infections(HPO:0002788) Abnormality of the respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory tract infection(HPO:0011947) Recurrent respiratory infections(HPO:0002205) Recurrent upper respiratory tract infections(HPO:0002788) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Recurrent infections(HPO:0002719) Recurrent respiratory infections(HPO:0002205) Recurrent upper respiratory tract infections(HPO:0002788) MedDRA: Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Recurrent upper respiratory tract infections(HPO:0002788) |
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Database Frequency: | 31 / 7739 | |||||||||||||||
Resource: |
All diseases associated with this symptom:
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE V | (OMIM:616100) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital laryngeal web | (Orphanet:2374) |
Desquamative interstitial pneumonia | (Orphanet:98852) |
Hurler syndrome | (Orphanet:93473) |
Hyper-IgM syndrome type 4 | (Orphanet:101091) |
Hypoplasminogenemia | (Orphanet:722) |
Immunodeficiency by defective expression of HLA class 2 | (Orphanet:572) |
Langer-Giedion syndrome | (Orphanet:502) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Ligneous conjunctivitis | (Orphanet:97231) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Mucopolysaccharidosis type 3 | (Orphanet:581) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
Mucopolysaccharidosis type 6 | (Orphanet:583) |
Obesity due to congenital leptin deficiency | (Orphanet:66628) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
Rubinstein-Taybi syndrome due to CREBBP mutations | (Orphanet:353277) |
Sanfilippo syndrome type A | (Orphanet:79269) |
Sanfilippo syndrome type B | (Orphanet:79270) |
Sanfilippo syndrome type C | (Orphanet:79271) |
Sanfilippo syndrome type D | (Orphanet:79272) |
Severe combined immunodeficiency due to DCLRE1C deficiency | (Orphanet:275) |
Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
T-B+ severe combined immunodeficiency due to JAK3 deficiency | (Orphanet:35078) |
WHIM syndrome | (Orphanet:51636) |
WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |