Pneumonia
Symptom Information:
| Symptom ID: | HPO:0002090 | ||||
| Synonyms: |
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| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the respiratory system(HPO:0002086) Abnormal respiratory system morphology(HPO:0012252) Abnormality of lung morphology(HPO:0002088) Respiratory tract infection(HPO:0011947) Pneumonia(HPO:0002090) MedDRA: Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Lower respiratory tract and lung infections(MedDRA:10025101) Pneumonia(HPO:0002090) |
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| Database Frequency: | 59 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| AGAMMAGLOBULINEMIA, X-LINKED | (OMIM:300755) |
| Acute interstitial pneumonia | (Orphanet:79126) |
| Alström syndrome | (Orphanet:64) |
| Autoimmune lymphoproliferative syndrome with recurrent infections | (Orphanet:275517) |
| Autosomal recessive limb-girdle muscular dystrophy type 2C | (Orphanet:353) |
| CHOLESTEROL PNEUMONIA | (OMIM:215030) |
| CILIARY DYSKINESIA, PRIMARY, 1 | (OMIM:244400) |
| COMBINED IMMUNODEFICIENCY, X-LINKED | (OMIM:312863) |
| COMPLEMENT FACTOR B DEFICIENCY | (OMIM:615561) |
| CORNELIA DE LANGE SYNDROME 1 | (OMIM:122470) |
| Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
| Combined immunodeficiency due to ZAP70 deficiency | (Orphanet:911) |
| Combined immunodeficiency with facio-oculo-skeletal anomalies | (Orphanet:221139) |
| Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
| Cornelia de Lange syndrome | (Orphanet:199) |
| Cryptosporidiosis - chronic cholangitis - liver disease | (Orphanet:357329) |
| Cyclic neutropenia | (Orphanet:2686) |
| Familial acute necrotizing encephalopathy | (Orphanet:88619) |
| Hereditary mucoepithelial dysplasia | (Orphanet:1839) |
| Heritable pulmonary arterial hypertension | (Orphanet:275777) |
| Hurler syndrome | (Orphanet:93473) |
| ICF syndrome | (Orphanet:2268) |
| IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
| IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME1 | (OMIM:242860) |
| IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2 | (OMIM:614069) |
| Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
| Idiopathic pulmonary fibrosis | (Orphanet:2032) |
| Kostmann syndrome | (Orphanet:99749) |
| LYMPHOPENIC HYPERGAMMAGLOBULINEMIA, ANTIBODY DEFICIENCY, AUTOIMMUNEHEMOLYTIC ANEMIA, AND GLOMERULONEPHRITIS | (OMIM:247800) |
| Leigh syndrome with nephrotic syndrome | (Orphanet:255249) |
| Leprechaunism | (Orphanet:508) |
| Leukocyte adhesion deficiency type II | (Orphanet:99843) |
| Lymphoid interstitial pneumonia | (Orphanet:79128) |
| MEGDEL syndrome | (Orphanet:352328) |
| MUSCULAR HYPERTONIA, LETHAL | (OMIM:254120) |
| Neutropenia, severe congenital, 1, autosomal dominant | (OMIM:202700) |
| Non-specific interstitial pneumonia | (Orphanet:91364) |
| Omenn syndrome | (Orphanet:39041) |
| Pediatric systemic lupus erythematosus | (Orphanet:93552) |
| Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
| Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
| Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
| Pyruvate carboxylase deficiency | (Orphanet:3008) |
| Pyruvate dehydrogenase E3-binding protein deficiency | (Orphanet:255182) |
| Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |
| SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
| Severe X-linked mitochondrial encephalomyopathy | (Orphanet:238329) |
| Severe combined immunodeficiency due to CARD11 deficiency | (Orphanet:357237) |
| Severe combined immunodeficiency due to DCLRE1C deficiency | (Orphanet:275) |
| Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
| Severe combined immunodeficiency due to complete RAG1/2 deficiency | (Orphanet:331206) |
| Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia | (Orphanet:632) |
| Simpson-Golabi-Behmel syndrome type 2 | (Orphanet:79022) |
| Susceptibility to chronic infection by Epstein-Barr virus | (Orphanet:2566) |
| T-B+ severe combined immunodeficiency due to JAK3 deficiency | (Orphanet:35078) |
| T-B+ severe combined immunodeficiency due to gamma chain deficiency | (Orphanet:276) |
| TENORIO SYNDROME | (OMIM:616260) |
| WISKOTT-ALDRICH SYNDROME | (OMIM:301000) |
| WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM | (OMIM:600903) |