Immunodeficiency
Symptom Information:
Symptom ID: | HPO:0002721 | ||||||||||||||||||||||
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 the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Immunodeficiency(HPO:0002721) MedDRA: Immune system disorders(MedDRA:10021428) Immunodeficiency syndromes(MedDRA:10021460) Immunodeficiency disorders NEC(MedDRA:10052739) Immunodeficiency(HPO:0002721) Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Infections NEC(MedDRA:10021902) Immunodeficiency(HPO:0002721) |
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Database Frequency: | 97 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema | (Orphanet:69088) |
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency | (Orphanet:331226) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Bloom syndrome | (Orphanet:125) |
CANDIDIASIS, FAMILIAL, 2 | (OMIM:212050) |
CD3 ANTIGEN, EPSILON SUBUNIT | (OMIM:186830) |
CD3 ANTIGEN, GAMMA SUBUNIT | (OMIM:186740) |
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME | (OMIM:215250) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Combined immunodeficiency due to STIM1 deficiency | (Orphanet:317430) |
Combined immunodeficiency due to STK4 deficiency | (Orphanet:314689) |
Common variable immunodeficiency | (Orphanet:1572) |
Cryptosporidiosis - chronic cholangitis - liver disease | (Orphanet:357329) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Facial dysmorphism - immunodeficiency - livedo - short stature | (Orphanet:352712) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
HYPERZINCEMIA WITH FUNCTIONAL ZINC DEPLETION | (OMIM:601979) |
Hepatic veno-occlusive disease - immunodeficiency | (Orphanet:79124) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
Hermansky-Pudlak syndrome with neutropenia | (Orphanet:183678) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hyper-IgM syndrome type 2 | (Orphanet:101089) |
Hyper-IgM syndrome type 3 | (Orphanet:101090) |
Hyper-IgM syndrome type 4 | (Orphanet:101091) |
Hyper-IgM syndrome type 5 | (Orphanet:101092) |
Hypohidrotic ectodermal dysplasia with immunodeficiency | (Orphanet:98813) |
ICF syndrome | (Orphanet:2268) |
IMMUNODEFICIENCY 12 | (OMIM:615468) |
IMMUNODEFICIENCY 14 | (OMIM:615513) |
IMMUNODEFICIENCY 15 | (OMIM:615592) |
IMMUNODEFICIENCY 16 | (OMIM:615593) |
IMMUNODEFICIENCY 17 | (OMIM:615607) |
IMMUNODEFICIENCY 18 | (OMIM:615615) |
IMMUNODEFICIENCY 19 | (OMIM:615617) |
IMMUNODEFICIENCY 20 | (OMIM:615707) |
IMMUNODEFICIENCY 22 | (OMIM:615758) |
IMMUNODEFICIENCY 23 | (OMIM:615816) |
IMMUNODEFICIENCY 25 | (OMIM:610163) |
IMMUNODEFICIENCY 28 | (OMIM:614889) |
IMMUNODEFICIENCY 29 | (OMIM:614890) |
IMMUNODEFICIENCY 30 | (OMIM:614891) |
IMMUNODEFICIENCY 31A | (OMIM:614892) |
IMMUNODEFICIENCY 31C | (OMIM:614162) |
IMMUNODEFICIENCY 36 | (OMIM:616005) |
IMMUNODEFICIENCY 37 | (OMIM:616098) |
IMMUNODEFICIENCY 38, WITH BASAL GANGLIA CALCIFICATION | (OMIM:616126) |
IMMUNODEFICIENCY WITH DEFECTIVE LEUKOCYTE AND LYMPHOCYTE FUNCTIONAND WITH RESPONSE TO HISTAMINE-1 ANTAGONIST | (OMIM:146840) |
IMMUNODEFICIENCY WITHOUT ANHIDROTIC ECTODERMAL DYSPLASIA | (OMIM:300584) |
IMMUNODEFICIENCY, COMMON VARIABLE, 1 | (OMIM:607594) |
IMMUNODEFICIENCY, COMMON VARIABLE, 10 | (OMIM:615577) |
IMMUNODEFICIENCY, COMMON VARIABLE, 11 | (OMIM:615767) |
IMMUNODEFICIENCY, COMMON VARIABLE, 2 | (OMIM:240500) |
IMMUNODEFICIENCY, COMMON VARIABLE, 3 | (OMIM:613493) |
IMMUNODEFICIENCY, COMMON VARIABLE, 4 | (OMIM:613494) |
IMMUNODEFICIENCY, COMMON VARIABLE, 5 | (OMIM:613495) |
IMMUNODEFICIENCY, COMMON VARIABLE, 6 | (OMIM:613496) |
IMMUNODEFICIENCY, COMMON VARIABLE, 7 | (OMIM:614699) |
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY | (OMIM:614700) |
IMMUNODEFICIENCY, PARTIAL COMBINED, WITH ABSENCE OF HLA DETERMINANTSAND BETA-2-MICROGLOBULIN FROM LYMPHOCYTES | (OMIM:242870) |
IMMUNODEFICIENCY, X-LINKED, WITH DEFICIENCY OF 115,000 DALTON SURFACEGLYCOPROTEIN | (OMIM:308220) |
IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME2 | (OMIM:614069) |
Idiopathic CD4 lymphocytopenia | (Orphanet:228000) |
Immunodeficiency due to CD25 deficiency | (Orphanet:169100) |
Immunodeficiency due to ficolin3 deficiency | (Orphanet:331190) |
Immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency | (Orphanet:70592) |
Intellectual deficit, X-linked, Wilson type | (Orphanet:85290) |
LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 1 | (OMIM:308240) |
Leigh syndrome | (Orphanet:506) |
Leprechaunism | (Orphanet:508) |
Lethal ataxia with deafness and optic atrophy | (Orphanet:1187) |
Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis | (Orphanet:137631) |
MEGDEL syndrome | (Orphanet:352328) |
MELAS | (Orphanet:550) |
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS | (OMIM:250460) |
Monocytopenia with susceptibility to infections | (Orphanet:228423) |
NEUTROPHIL MIGRATION | (OMIM:162820) |
Neutrophil immunodeficiency syndrome | (Orphanet:183707) |
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY | (OMIM:615895) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polyglucosan body myopathy type 1 | (ORPHA:397937) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
RIDDLE SYNDROME | (OMIM:611943) |
Reticular dysgenesis | (Orphanet:33355) |
Severe combined immunodeficiency due to CARD11 deficiency | (Orphanet:357237) |
Severe combined immunodeficiency due to CORO1A deficiency | (Orphanet:228003) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |
TRICHOHEPATOENTERIC SYNDROME 2 | (OMIM:614602) |
Timothy syndrome | (Orphanet:65283) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |
X-linked hyper-IgM syndrome | (Orphanet:101088) |
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia | (Orphanet:317476) |
X-linked mendelian susceptibility to mycobacterial diseases | (Orphanet:319605) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |