Abnormality of immune system physiology

Symptom Information:

Symptom ID: HPO:0010978
Cross references:
Is a (Direct Parents):
HPO         Abnormality of the immune system
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of immune system physiology(HPO:0010978)
Database Frequency: 148 / 7739

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)