Abnormality of the immune system

Symptom Information:

Symptom ID: HPO:0002715
Synonyms:
Immunological abnormality [HPO:0002715]
Immune system anomaly [Orphanet:47000]
Anomalies of the immunitary system [Orphanet:47000]
Quality:
Cross references:
Orphanet:47000 "Anomalies of the immunitary system" [Orphanet:47000]
Is a (Direct Parents):
HPO         Phenotypic abnormality
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
MedDRA:
Database Frequency: 46 / 7739
Resource:

All diseases associated with this symptom:

Allergic bronchopulmonary aspergillosis (Orphanet:1164)
Ataxia-telangiectasia (Orphanet:100)
Autosomal dominant hyper-IgE syndrome (Orphanet:2314)
BLOOD GROUP, DUFFY SYSTEM (OMIM:110700)
CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 1 (OMIM:302650)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies (Orphanet:95715)
DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF (OMIM:125260)
DEND syndrome (Orphanet:79134)
DIABETES MELLITUS, INSULIN-DEPENDENT (OMIM:222100)
ECHO VIRUS 11 SENSITIVITY (OMIM:129150)
EOSINOPHILOPENIA (OMIM:131430)
Epidermodysplasia verruciformis (Orphanet:302)
GLOBULIN ANOMALY INVOLVING BETA (2A)-GLOBULIN (OMIM:137900)
Hereditary folate malabsorption (Orphanet:90045)
IMMUNE SUPPRESSION (OMIM:146850)
IMMUNOGLOBULIN D LEVEL IN PLASMA, LOW (OMIM:242890)
INOSINE PHOSPHORYLASE DEFICIENCY, IMMUNE DEFECT DUE TO (OMIM:243080)
INTRINSIC FACTOR DEFICIENCY (OMIM:261000)
Isolated growth hormone deficiency type IA (Orphanet:231662)
LYSINE-SPECIFIC DEMETHYLASE 5D (OMIM:426000)
Leprosy (Orphanet:548)
Lymphoid interstitial pneumonia (Orphanet:79128)
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS (OMIM:250460)
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY (OMIM:608931)
Monomelic amyotrophy (Orphanet:65684)
Multiple carboxylase deficiency (Orphanet:148)
Myeloperoxidase deficiency (Orphanet:2587)
Navajo neurohepatopathy (Orphanet:255229)
POLIOVIRUS RECEPTOR (OMIM:173850)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Postsynaptic congenital myasthenic syndromes (Orphanet:98913)
Presynaptic congenital myasthenic syndromes (Orphanet:98914)
RADIATION SENSITIVITY OF NATURAL KILLER ACTIVITY (OMIM:312210)
RAGWEED SENSITIVITY (OMIM:179450)
RHEUMATOID ARTHRITIS (OMIM:180300)
Reticular dysgenesis (Orphanet:33355)
Rheumatic fever (Orphanet:3099)
Roussy-Lévy syndrome (Orphanet:3115)
SHORT syndrome (Orphanet:3163)
SURFACTANT, PULMONARY-ASSOCIATED PROTEIN D (OMIM:178635)
SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS (OMIM:272370)
Schistosomiasis (Orphanet:1247)
Synaptic congenital myasthenic syndromes (Orphanet:98915)
Syndromic diarrhea (Orphanet:84064)
Wolf-Hirschhorn syndrome (Orphanet:280)