Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

62 matching diseasesClear search ×

Primary immunodeficiency

ORPHA:101997

Primary immunodeficiency due to a defect in adaptive immunity

ORPHA:179006

Primary immunodeficiency due to a defect in innate immunity

ORPHA:101988

Primary immunodeficiency syndrome due to P14/LAMTOR2 deficiency

Primary immunodeficiency syndrome due to P14 deficiency · Primary immunodeficiency syndrome due to LAMTOR2 deficiency

ORPHA:90023

Primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency

Primary immunodeficiency due to MCM4 deficiency

ORPHA:75391

Primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection

Primary immunodeficiency with post-MMR vaccine viral infection

ORPHA:431166

Primary immunodeficiency with predisposition to severe viral infection

ORPHA:431156

Mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency

MSMD due to complete RORgamma receptor defiency · Primary immunodeficiency due to RORC mutation

ORPHA:477857

NIK deficiency

Primary immunodeficiency with multifaceted aberrant lymphoid immunity

ORPHA:447731

Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency

Evans syndrome associated with primary immunodeficiency · TPPII-related immunodeficiency, autoimmunity, and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease

ORPHA:444463

Autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity

Autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity · CD16 deficiency

ORPHA:437552

OBSOLETE: Other complex syndrome of primary immunodeficiency

ORPHA:183716

Acquired immunodeficiency

ORPHA:310050

Addison disease

Primary Addison disease · Autoimmune adrenalitis

ORPHA:85138

Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies

Acquired adult-onset immunodeficiency · Adult-onset immunodeficiency with acquired anti-interferon-gamma autoantibodies

ORPHA:306431

Coenzyme Q10 deficiency

Primary coenzyme Q10 deficiency · CoQ10 deficiency

ORPHA:35656

Combined immunodeficiency due to c-REL deficiency

CID due to c-REL deficiency · Combined immunodeficiency due to cellular homolog of v-Rel deficiency

ORPHA:697394

Combined immunodeficiency due to CARD11 deficiency

CID due to CARD11 deficiency · Combined immunodeficiency due to caspase recruitment domain family member 11 protein deficiency

ORPHA:357237

Combined immunodeficiency due to CD27 deficiency

CD27 deficiency · Autosomal recessive lymphoproliferative disease due to CD27 deficiency

ORPHA:238505

Combined immunodeficiency due to DOCK2 deficiency

Combined immunodeficiency due to dedicator of cytokinesis 2 protein deficiency · CID due to DOCK2 deficiency

ORPHA:447737

Combined immunodeficiency due to DOCK8 deficiency

CID due to DOCK8 deficiency · Combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency

ORPHA:217390

Combined immunodeficiency due to FCHO1 deficiency

ORPHA:647804

Combined immunodeficiency due to GINS1 deficiency

Combined immunodeficiency with intrauterine growth retardation-natural killer cell deficiency-neutropenia · CID due to GINS1 deficiency

ORPHA:505227

Combined immunodeficiency due to HELIOS deficiency

CID due to HELIOS deficiency · Combined immunodeficiency due to IKZF2 deficiency

ORPHA:697389

Combined immunodeficiency due to IKBKB deficiency

CID due to IKBKB deficiency · Combined immunodeficiency due to inhibitor of nuclear factor kappa B subunit beta deficiency

ORPHA:397787

Combined immunodeficiency due to IL21R deficiency

CID due to IL21R deficiency · Combined immunodeficiency due to interleukin 21 receptor deficiency

ORPHA:357329

Combined immunodeficiency due to ITK deficiency

ITK deficiency · Autosomal recessive lymphoproliferative disease due to ITK deficiency

ORPHA:538963

Combined immunodeficiency due to LCK deficiency

CID due to LCK deficiency · CID due to lymphocyte-specific protein tyrosine kinase deficiency

ORPHA:280142

Combined immunodeficiency due to MALT1 deficiency

ORPHA:397964

Combined immunodeficiency due to Moesin deficiency

MSN-related combined immunodeficiency · CID due to Moesin deficiency

ORPHA:504530

Combined immunodeficiency due to ORAI1 deficiency

CID due to ORAI1 deficiency

ORPHA:317428

Combined immunodeficiency due to OX40 deficiency

Combined immunodeficiency with childhood-onset Kaposi sarcoma · Combined immunodeficiency with impaired immunity to HHV-8

ORPHA:431149

Combined immunodeficiency due to RELB deficiency

CID due to RELB deficiency · Combined immunodeficiency due to RELB proto-oncogene NF-kB subunit deficiency

ORPHA:688594

Combined immunodeficiency due to STIM1 deficiency

CID due to STIM1 deficiency

ORPHA:317430

Combined immunodeficiency due to STK4 deficiency

CID due to STK4 deficiency

ORPHA:314689

Combined immunodeficiency due to TBX1 deficiency

ORPHA:685017

Combined immunodeficiency due to TFRC deficiency

CID due to TFRC deficiency · TFRC-related combined immunodeficiency

ORPHA:476113

Combined immunodeficiency due to ZAP70 deficiency

Zeta-associated-protein 70 deficiency

ORPHA:911

Combined T and B cell immunodeficiency

ORPHA:101972

FADD-related immunodeficiency

ORPHA:306550

Griscelli syndrome

Chédiak-Higashi-like syndrome · Griscelli-Pruniéras syndrome

ORPHA:381

Immunodeficiency due to CD25 deficiency

Interleukin-2 receptor alpha chain deficiency

ORPHA:169100

Immunodeficiency due to ficolin3 deficiency

ORPHA:331190

Immunodeficiency due to MASP-2 deficiency

ORPHA:331187

Immunodeficiency with factor H anomaly

ORPHA:200421

Immunodeficiency with factor I anomaly

Complete factor I deficiency

ORPHA:200418

Laron syndrome with immunodeficiency

Laron-like syndrome · Short stature due to STAT5b deficiency

ORPHA:220465

Non-severe combined immunodeficiency

Non-SCID

ORPHA:480549