Abnormality of immune system physiology
Symptom Information:
| Symptom ID: | HPO:0010978 | ||
| Synonyms: |
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| Quality: | |||
| 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) MedDRA: |
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| Database Frequency: | 148 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| 15q14 microdeletion syndrome | (Orphanet:261190) |
| 15q24 microdeletion syndrome | (Orphanet:94065) |
| 1p36 deletion syndrome | (Orphanet:1606) |
| 22q11.2 deletion syndrome | (Orphanet:567) |
| 22q11.2 microduplication syndrome | (Orphanet:1727) |
| ACTH-dependent Cushing syndrome | (Orphanet:99892) |
| ALG1-CDG | (Orphanet:79327) |
| ALG12-CDG | (Orphanet:79324) |
| Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
| Acrodysostosis | (Orphanet:950) |
| Alopecia antibody deficiency | (Orphanet:1006) |
| Alpha heavy-chain disease | (Orphanet:100025) |
| Alpha-thalassemia | (Orphanet:846) |
| Alpha-thalassemia - myelodysplastic syndrome | (Orphanet:231401) |
| Arachnodactyly - intellectual deficit - dysmorphism | (Orphanet:1130) |
| Ataxia-telangiectasia | (Orphanet:100) |
| Attenuated Chédiak-Higashi syndrome | (Orphanet:352723) |
| Autoimmune hemolytic anemia | (Orphanet:98375) |
| Autosomal agammaglobulinemia | (Orphanet:33110) |
| Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
| Autosomal recessive spondylocostal dysostosis | (Orphanet:2311) |
| Babesiosis | (Orphanet:108) |
| Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
| Bullous pemphigoid | (Orphanet:703) |
| C syndrome | (Orphanet:1308) |
| CHARGE syndrome | (Orphanet:138) |
| COFS syndrome | (Orphanet:1466) |
| COG7-CDG | (Orphanet:79333) |
| Cabezas syndrome | (Orphanet:85293) |
| Cernunnos-XLF deficiency | (Orphanet:169079) |
| Cheilitis glandularis | (Orphanet:1221) |
| Chronic granulomatous disease | (Orphanet:379) |
| Chronic mucocutaneous candidiasis | (Orphanet:1334) |
| Chédiak-Higashi syndrome | (Orphanet:167) |
| Combined immunodeficiency T+ B+ due to partial RAG1 deficiency | (Orphanet:231154) |
| Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
| Common variable immunodeficiency | (Orphanet:1572) |
| Congenital atransferrinemia | (Orphanet:1195) |
| Congenital disorder of glycosylation | (Orphanet:137) |
| Congenital erythropoietic porphyria | (Orphanet:79277) |
| Congenital lobar emphysema | (Orphanet:1928) |
| Cronkhite-Canada syndrome | (Orphanet:2930) |
| Cushing disease | (Orphanet:96253) |
| Cushing syndrome | (Orphanet:553) |
| Cushing syndrome due to ectopic ACTH secretion | (Orphanet:99889) |
| Cystic fibrosis | (Orphanet:586) |
| Developmental malformations - deafness - dystonia | (Orphanet:79107) |
| Distal 22q11.2 microdeletion syndrome | (Orphanet:261330) |
| Distal monosomy 7q36 | (Orphanet:1636) |
| Down syndrome | (Orphanet:870) |
| Dubowitz syndrome | (Orphanet:235) |
| Dyskeratosis congenita | (Orphanet:1775) |
| Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
| Ectodermal dysplasia syndrome | (Orphanet:79373) |
| Epidermolysis bullosa simplex due to plakophilin deficiency | (Orphanet:158668) |
| Erdheim-Chester disease | (Orphanet:35687) |
| Erythroderma desquamativum | (Orphanet:314) |
| Familial benign copper deficiency | (Orphanet:1551) |
| Felty syndrome | (Orphanet:47612) |
| Fetal alcohol syndrome | (Orphanet:1915) |
| Floating-Harbor syndrome | (Orphanet:2044) |
| GM1 gangliosidosis | (Orphanet:354) |
| Galloway-Mowat syndrome | (Orphanet:2065) |
| Ghosal hematodiaphyseal dysplasia | (Orphanet:1802) |
| Glutathione synthetase deficiency | (Orphanet:32) |
| Glycogen storage disease due to glucose-6-phosphatase deficiency | (Orphanet:364) |
| Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
| Griscelli disease | (Orphanet:381) |
| Griscelli disease type 2 | (Orphanet:79477) |
| Growth hormone insensitivity syndrome | (Orphanet:181393) |
| Hair defect - photosensitivity - intellectual deficit | (Orphanet:1408) |
| Hairy cell leukemia variant | (Orphanet:300878) |
| Hemoglobin E - beta-thalassemia | (Orphanet:231249) |
| Hennekam syndrome | (Orphanet:2136) |
| Hereditary folate malabsorption | (Orphanet:90045) |
| Hereditary orotic aciduria | (Orphanet:30) |
| Hermansky-Pudlak syndrome | (Orphanet:79430) |
| Hodgkin lymphoma | (Orphanet:98293) |
| Hodgkin lymphoma, classical | (Orphanet:391) |
| Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
| Hydrocephalus - blue sclerae - nephropathy | (Orphanet:2186) |
| Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
| Hypohidrotic ectodermal dysplasia | (Orphanet:238468) |
| ICF syndrome | (Orphanet:2268) |
| Ichthyosis follicularis - alopecia - photophobia | (Orphanet:2273) |
| Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency | (Orphanet:70592) |
| Incontinentia pigmenti | (Orphanet:464) |
| Intellectual deficit - hypoplastic corpus callosum - preauricular tag | (Orphanet:1495) |
| Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
| Intellectual deficit, X-linked, Pai type | (Orphanet:85322) |
| Isolated agammaglobulinemia | (Orphanet:229717) |
| Jacobsen syndrome | (Orphanet:2308) |
| KID syndrome | (Orphanet:477) |
| Kabuki syndrome | (Orphanet:2322) |
| LIG4 syndrome | (Orphanet:99812) |
| Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
| Leukocyte adhesion deficiency | (Orphanet:2968) |
| Lichstenstein syndrome | (Orphanet:2390) |
| Low birth weight - dwarfism - dysgammaglobulinemia | (Orphanet:2621) |
| MELAS | (Orphanet:550) |
| Malakoplakia | (Orphanet:556) |
| Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
| Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency | (Orphanet:319600) |
| Monosomy 22q13 | (Orphanet:48652) |
| Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
| Mucopolysaccharidosis type 2 | (Orphanet:580) |
| Natal teeth - intestinal pseudoobstruction - patent ductus | (Orphanet:1654) |
| Netherton syndrome | (Orphanet:634) |
| Neutropenia - monocytopenia - deafness | (Orphanet:2690) |
| Neutrophil immunodeficiency syndrome | (Orphanet:183707) |
| Nodular lymphocyte predominant Hodgkin lymphoma | (Orphanet:86893) |
| Norrie disease | (Orphanet:649) |
| Oculocerebral hypopigmentation syndrome, Preus type | (Orphanet:2720) |
| Osteopetrosis | (Orphanet:2781) |
| Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
| Pemphigus vulgaris | (Orphanet:704) |
| Pentasomy X | (Orphanet:11) |
| Primary effusion lymphoma | (Orphanet:48686) |
| Primary immunodeficiency syndrome due to p14 deficiency | (Orphanet:90023) |
| Primary intestinal lymphangiectasia | (Orphanet:90362) |
| Progeria - short stature - pigmented nevi | (Orphanet:2959) |
| Prolidase deficiency | (Orphanet:742) |
| Propionic acidemia | (Orphanet:35) |
| Proteus syndrome | (Orphanet:744) |
| Pyogenic bacterial infections due to MyD88 deficiency | (Orphanet:183713) |
| Pyomyositis | (Orphanet:764) |
| Reticular dysgenesis | (Orphanet:33355) |
| Say-Barber-Miller syndrome | (Orphanet:3132) |
| Schwartz-Jampel syndrome | (Orphanet:800) |
| Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy | (Orphanet:169095) |
| Severe combined immunodeficiency | (Orphanet:183660) |
| Short stature - deafness - neutrophil dysfunction - dysmorphism | (Orphanet:2866) |
| Short-limb skeletal dysplasia with severe combined immunodeficiency | (Orphanet:935) |
| Shwachman-Diamond syndrome | (Orphanet:811) |
| Smith-Lemli-Opitz syndrome | (Orphanet:818) |
| Sotos syndrome | (Orphanet:821) |
| Sézary syndrome | (Orphanet:3162) |
| Tetrasomy X | (Orphanet:9) |
| Thymic tumor | (Orphanet:100100) |
| Triose phosphate-isomerase deficiency | (Orphanet:868) |
| Vici syndrome | (Orphanet:1493) |
| Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
| Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
| Waldenström macroglobulinemia | (Orphanet:33226) |
| Wiskott-Aldrich syndrome | (Orphanet:906) |
| Wolcott-Rallison syndrome | (Orphanet:1667) |
| X-linked agammaglobulinemia | (Orphanet:47) |
| Yellow nail syndrome | (Orphanet:662) |