Immunodeficiency due to a complement regulatory deficiency
ORPHA:459348Immunodeficiency due to a late component of complement deficiency
ORPHA:169150Immunodeficiency due to CD25 deficiency
ORPHA:169100Immunodeficiency with factor I anomaly
ORPHA:200418Isolated complex I deficiency
ORPHA:2609Isolated complex III deficiency
ORPHA:1460Late-onset combined immunodeficiency due to ICOS deficiency
ORPHA:695183Late-onset combined immunodeficiency due to ICOSL deficiency
ORPHA:695191Lesch-Nyhan syndrome
ORPHA:510Limb-girdle muscular dystrophy due to POMK deficiency
ORPHA:445110Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency
ORPHA:99898Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
ORPHA:319547Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency
ORPHA:319558Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency
ORPHA:319552Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency
ORPHA:319563Mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
ORPHA:477857Mevalonic aciduria
ORPHA:29Obesity due to CEP19 deficiency
ORPHA:397615OBSOLETE: Common variable immunodeficiency due to TNFR deficiency
ORPHA:183672PGM3-CDG
ORPHA:443811Postural orthostatic tachycardia syndrome due to NET deficiency
ORPHA:443236Severe combined immunodeficiency due to complete RAG1/2 deficiency
ORPHA:331206Severe combined immunodeficiency due to CORO1A deficiency
ORPHA:228003Severe combined immunodeficiency due to CTPS1 deficiency
ORPHA:420573Severe combined immunodeficiency due to DCLRE1C deficiency
ORPHA:275Severe combined immunodeficiency due to DNA-PKcs deficiency
ORPHA:317425Severe combined immunodeficiency due to FOXN1 deficiency
ORPHA:169095Severe combined immunodeficiency due to LAT deficiency
ORPHA:504523Severe congenital neutropenia due to G6PC3 deficiency
ORPHA:331176Severe congenital neutropenia due to JAGN1 deficiency
ORPHA:423384Severe mendelian susceptibility to mycobacterial diseases due to complete IFNG deficiency
ORPHA:699618Severe mendelian susceptibility to mycobacterial diseases due to complete IRF1 deficiency
ORPHA:699615T-B+ severe combined immunodeficiency due to CD45 deficiency
ORPHA:169157T-B+ severe combined immunodeficiency due to gamma chain deficiency
ORPHA:276T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency
ORPHA:169154T-B+ severe combined immunodeficiency due to JAK3 deficiency
ORPHA:35078X-linked combined immunodeficiency due to SASH3 deficiency
ORPHA:653751XMEN
ORPHA:317476