| Source | Code | Name | Case count | Share of cases (%) |
|---|---|---|---|---|
| OUTPAT | OUTPAT_ICD10(D860) | Sarcoidosis of lung | 1258 | |
| OUTPAT | OUTPAT_ICD10(D868) | Sarcoidosis of other and combined sites | 911 | |
| OUTPAT | OUTPAT_ICD10(D862) | Sarcoidosis of lung with sarcoidosis of lymph nodes | 864 | |
| OUTPAT | OUTPAT_ICD10(D869) | Sarcoidosis, unspecified | 725 | |
| OUTPAT | OUTPAT_ICD10(D861) | Sarcoidosis of lymph nodes | 578 | |
| OUTPAT | OUTPAT_ICD10(D8980) | Immunoglobulin A (IgA) deposits in organisms | 540 | |
| INPAT | INPAT_ICD8(13597) | Sarcoidosis, Suspecta | 410 | |
| INPAT | INPAT_ICD10(D860) | Sarcoidosis of lung | 385 | |
| INPAT | INPAT_ICD10(D868) | Sarcoidosis of other and combined sites | 364 | |
| INPAT | INPAT_ICD8(13599) | Sarcoidosis, Unspecified | 353 | |
| INPAT | INPAT_ICD9(1350A) | Sarcoidosis | 313 | |
| INPAT | INPAT_ICD10(D8980) | Immunoglobulin A (IgA) deposits in organisms | 307 | |
| REIMB | REIMB_KELA(132)_ICD10(D86) | Sarcoidosis, Sarcoidosis | 279 | |
| OUTPAT | OUTPAT_ICD10(D801) | Nonfamilial hypogammaglobulinaemia | 246 | |
| OUTPAT | OUTPAT_ICD10(D863) | Sarcoidosis of skin | 244 | |
| INPAT | INPAT_ICD10(D869) | Sarcoidosis, unspecified | 238 | |
| OUTPAT | OUTPAT_ICD10(D809) | Immunodeficiency with predominantly antibody defects, unspecified | 187 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D860) | Sarcoidosis of lung. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 179 | |
| REIMB | REIMB_KELA(132)_ICD8(NA) | Sarcoidosis, Name not found | 176 | |
| INPAT | INPAT_ICD10(D862) | Sarcoidosis of lung with sarcoidosis of lymph nodes | 174 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8980) | Immunoglobulin A (IgA) deposits in organisms. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 167 | |
| OUTPAT | OUTPAT_ICD10(D803) | Selective deficiency of immunoglobulin G [IgG] subclasses | 166 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D868) | Sarcoidosis of other and combined sites. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 160 | |
| OUTPAT | OUTPAT_ICD10(D808) | Other immunodeficiencies with predominantly antibody defects | 140 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D86) | Sarcoidosis. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 132 | |
| INPAT | INPAT_ICD10(D801) | Nonfamilial hypogammaglobulinaemia | 125 | |
| INPAT | INPAT_ICD10(D861) | Sarcoidosis of lymph nodes | 104 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D862) | Sarcoidosis of lung with sarcoidosis of lymph nodes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 92 | |
| REIMB | REIMB_KELA(132)_ICD9(NA) | Sarcoidosis, Name not found | 84 | |
| OUTPAT | OUTPAT_ICD10(D800) | Hereditary hypogammaglobulinaemia | 81 | |
| OUTPAT | OUTPAT_ICD10(D802) | Selective deficiency of immunoglobulin A [IgA] | 79 | |
| OUTPAT | OUTPAT_ICD10(D8989) | Other specified disorders involving the immune mechanism, not elsewhere classified | 75 | |
| OUTPAT | OUTPAT_ICD10(D814) | Nezelof's syndrome | 69 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D869) | Sarcoidosis, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 68 | |
| OUTPAT | OUTPAT_ICD10(D8418) | Other specified defect in the complement system | 67 | |
| REIMB | REIMB_KELA(120)_ICD10(D80) | Hypogammaglobulinaemia, Immunodeficiency with predominantly antibody defects | 63 | |
| OUTPAT | OUTPAT_ICD10(D849) | Immunodeficiency, unspecified | 60 | |
| INPAT | INPAT_ICD10(D810) | Severe combined immunodeficiency [SCID] with reticular dysgenesis | 59 | |
| INPAT | INPAT_ICD10(D809) | Immunodeficiency with predominantly antibody defects, unspecified | 58 | |
| OUTPAT | OUTPAT_ICD10(D830) | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function | 57 | |
| OUTPAT | OUTPAT_ICD10(D839) | Common variable immunodeficiency, unspecified | 57 | |
| INPAT | INPAT_ICD10(D814) | Nezelof's syndrome | 56 | |
| OUTPAT | OUTPAT_ICD10(D899) | Disorder involving the immune mechanism, unspecified | 51 | |
| OUTPAT | OUTPAT_ICD10(D841) | Defects in the complement system | 49 | |
| INPAT | INPAT_ICD10(D803) | Selective deficiency of immunoglobulin G [IgG] subclasses | 48 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D861) | Sarcoidosis of lymph nodes. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 47 | |
| REIMB | REIMB_KELA(132)_ICD10(D868) | Sarcoidosis, Sarcoidosis of other and combined sites | 46 | |
| OUTPAT | OUTPAT_ICD10(D8419) | Unspecified defect in the complement system | 45 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D801) | Nonfamilial hypogammaglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 43 | |
| REIMB | REIMB_KELA(120)_ICD10(D801) | Hypogammaglobulinaemia, Nonfamilial hypogammaglobulinaemia | 40 | |
| INPAT | INPAT_ICD10(D808) | Other immunodeficiencies with predominantly antibody defects | 35 | |
| REIMB | REIMB_KELA(132)_ICD10(D862) | Sarcoidosis, Sarcoidosis of lung with sarcoidosis of lymph nodes | 35 | |
| INPAT | INPAT_ICD10(D8989) | Other specified disorders involving the immune mechanism, not elsewhere classified | 32 | |
| OUTPAT | OUTPAT_ICD10(D806) | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia | 32 | |
| OUTPAT | OUTPAT_ICD10(D898) | Name not found | 32 | |
| INPAT | INPAT_ICD10(D839) | Common variable immunodeficiency, unspecified | 30 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D803) | Selective deficiency of immunoglobulin G [IgG] subclasses. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 30 | |
| OUTPAT | OUTPAT_ICD10(D810) | Severe combined immunodeficiency [SCID] with reticular dysgenesis | 29 | |
| INPAT | INPAT_ICD10(D863) | Sarcoidosis of skin | 28 | |
| OUTPAT | OUTPAT_ICD10(D838) | Other common variable immunodeficiencies | 27 | |
| OUTPAT | OUTPAT_ICD10(D891) | Cryoglobulinaemia | 27 | |
| OUTPAT | OUTPAT_ICD10(D8982) | Disease caused by deposition of the light chain of the immunoglobulins | 27 | |
| INPAT | INPAT_ICD10(D802) | Selective deficiency of immunoglobulin A [IgA] | 25 | |
| OUTPAT | OUTPAT_ICD10(D8411) | Hereditary angioedema type I | 24 | |
| REIMB | REIMB_KELA(132)_ICD10(D860) | Sarcoidosis, Sarcoidosis of lung | 24 | |
| OUTPAT | OUTPAT_ICD10(D848) | Other specified immunodeficiencies | 23 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D808) | Other immunodeficiencies with predominantly antibody defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 23 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D809) | Immunodeficiency with predominantly antibody defects, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 23 | |
| OUTPAT | OUTPAT_ICD10(D831) | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | 22 | |
| OUTPAT | OUTPAT_ICD10(D86) | Sarcoidosis | 22 | |
| OUTPAT | OUTPAT_ICD10(D818) | Other combined immunodeficiencies | 21 | |
| OUTPAT | OUTPAT_ICD10(D892) | Hypergammaglobulinaemia, unspecified | 21 | |
| INPAT | INPAT_ICD10(D800) | Hereditary hypogammaglobulinaemia | 20 | |
| OUTPAT | OUTPAT_ICD10(D819) | Combined immunodeficiency, unspecified | 19 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D863) | Sarcoidosis of skin. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 19 | |
| INPAT | INPAT_ICD9(2790B) | Disorders involving the immune mechanism, Deficiency of humoral immunity | 18 | |
| INPAT | INPAT_ICD10(D806) | Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia | 17 | |
| INPAT | INPAT_ICD10(D849) | Immunodeficiency, unspecified | 17 | |
| INPAT | INPAT_ICD10(D899) | Disorder involving the immune mechanism, unspecified | 17 | |
| INPAT | INPAT_ICD9(2790C) | Disorders involving the immune mechanism, Deficiency of humoral immunity | 17 | |
| OUTPAT | OUTPAT_ICD10(D890) | Polyclonal hypergammaglobulinaemia | 17 | |
| REIMB | REIMB_KELA(132)_ICD9(1350A) | Sarcoidosis, Sarcoidosis | 17 | |
| INPAT | INPAT_ICD10(D818) | Other combined immunodeficiencies | 16 | |
| OUTPAT | OUTPAT_ICD10(D811) | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers | 16 | |
| REIMB | REIMB_KELA(120)_ICD10(D808) | Hypogammaglobulinaemia, Other immunodeficiencies with predominantly antibody defects | 16 | |
| INPAT | INPAT_ICD10(D840) | Lymphocyte function antigen-1 [LFA-1] defect | 15 | |
| INPAT | INPAT_ICD10(D8982) | Disease caused by deposition of the light chain of the immunoglobulins | 15 | |
| OUTPAT | OUTPAT_ICD10(D8413) | Hereditary angioedema type III | 15 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D802) | Selective deficiency of immunoglobulin A [IgA]. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 15 | |
| REIMB | REIMB_KELA(120)_ICD10(D809) | Hypogammaglobulinaemia, Immunodeficiency with predominantly antibody defects, unspecified | 15 | |
| REIMB | REIMB_KELA(120)_ICD8(NA) | Hypogammaglobulinaemia, Name not found | 15 | |
| INPAT | INPAT_ICD10(D830) | Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function | 14 | |
| INPAT | INPAT_ICD10(D838) | Other common variable immunodeficiencies | 14 | |
| INPAT | INPAT_ICD10(D890) | Polyclonal hypergammaglobulinaemia | 14 | |
| OUTPAT | OUTPAT_ICD10(D824) | Hyperimmunoglobulin E [IgE] syndrome | 14 | |
| DEATH | DEATH_ICD10(D868) | Sarcoidosis of other and combined sites | 13 | |
| INPAT | INPAT_ICD10(D891) | Cryoglobulinaemia | 13 | |
| DEATH | DEATH_ICD10(D860) | Sarcoidosis of lung | 12 | |
| DEATH | DEATH_ICD10(D898) | Name not found | 12 | |
| INPAT | INPAT_ICD10(D831) | Common variable immunodeficiency with predominant immunoregulatory T-cell disorders | 12 | |
| INPAT | INPAT_ICD10(D8418) | Other specified defect in the complement system | 12 | |
| OUTPAT | OUTPAT_ICD10(D840) | Lymphocyte function antigen-1 [LFA-1] defect | 12 | |
| REIMB | REIMB_KELA(132)_ICD9(135) | Sarcoidosis, Sarcoidosis | 12 | |
| OUTPAT | OUTPAT_ICD10(D804) | Selective deficiency of immunoglobulin M [IgM] | 11 | |
| OUTPAT | OUTPAT_ICD10(D821) | Di George's syndrome | 11 | |
| OUTPAT | OUTPAT_ICD10(D822) | Immunodeficiency with short-limbed stature | 11 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D800) | Hereditary hypogammaglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 11 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8418) | Other specified defect in the complement system. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 11 | |
| REIMB | REIMB_KELA(120)_ICD10(D803) | Hypogammaglobulinaemia, Selective deficiency of immunoglobulin G [IgG] subclasses | 11 | |
| REIMB | REIMB_KELA(120)_ICD10(D83) | Hypogammaglobulinaemia, Common variable immunodeficiency | 11 | |
| INPAT | INPAT_ICD10(D812) | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers | 10 | |
| INPAT | INPAT_ICD10(D841) | Defects in the complement system | 10 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D89) | Other disorders involving the immune mechanism, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 10 | |
| REIMB | REIMB_KELA(120)_ICD10(D839) | Hypogammaglobulinaemia, Common variable immunodeficiency, unspecified | 10 | |
| REIMB | REIMB_KELA(132)_ICD9(1350) | Sarcoidosis, Name not found | 10 | |
| INPAT | INPAT_ICD9(2790A) | Disorders involving the immune mechanism, Deficiency of humoral immunity | 9 | |
| OUTPAT | OUTPAT_ICD10(D8412) | Hereditary angioedema type II | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D82) | Immunodeficiency associated with other major defects. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D839) | Common variable immunodeficiency, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 9 | |
| DEATH | DEATH_ICD10(D801) | Nonfamilial hypogammaglobulinaemia | 8 | |
| INPAT | INPAT_ICD10(D819) | Combined immunodeficiency, unspecified | 8 | |
| INPAT | INPAT_ICD10(D824) | Hyperimmunoglobulin E [IgE] syndrome | 8 | |
| INPAT | INPAT_ICD10(D8411) | Hereditary angioedema type I | 8 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D849) | Immunodeficiency, unspecified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 8 | |
| INPAT | INPAT_ICD10(D822) | Immunodeficiency with short-limbed stature | 7 | |
| INPAT | INPAT_ICD10(D828) | Immunodeficiency associated with other specified major defects | 7 | |
| INPAT | INPAT_ICD10(D8419) | Unspecified defect in the complement system | 7 | |
| INPAT | INPAT_ICD10(D848) | Other specified immunodeficiencies | 7 | |
| OUTPAT | OUTPAT_ICD10(D805) | Immunodeficiency with increased immunoglobulin M [IgM] | 7 | |
| OUTPAT | OUTPAT_ICD10(D828) | Immunodeficiency associated with other specified major defects | 7 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D848) | Other specified immunodeficiencies. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 7 | |
| REIMB | REIMB_KELA(120)_ICD10(D830) | Hypogammaglobulinaemia, Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function | 7 | |
| REIMB | REIMB_KELA(120)_ICD9(NA) | Hypogammaglobulinaemia, Name not found | 7 | |
| REIMB | REIMB_KELA(132)_ICD10(NA) | Sarcoidosis, Name not found | 7 | |
| INPAT | INPAT_ICD10(D811) | Severe combined immunodeficiency [SCID] with low T- and B-cell numbers | 6 | |
| INPAT | INPAT_ICD10(D813) | Adenosine deaminase [ADA] deficiency | 6 | |
| INPAT | INPAT_ICD10(D8413) | Hereditary angioedema type III | 6 | |
| OUTPAT | OUTPAT_ICD10(D812) | Severe combined immunodeficiency [SCID] with low or normal B-cell numbers | 6 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D891) | Cryoglobulinaemia. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 6 | |
| INPAT | INPAT_ICD10(D821) | Di George's syndrome | 5 | |
| INPAT | INPAT_ICD10(D892) | Hypergammaglobulinaemia, unspecified | 5 | |
| INPAT | INPAT_ICD8(13500) | Name not found | 5 | |
| INPAT | INPAT_ICD9(2798X) | Disorders involving the immune mechanism, Other specified disorders involving the immune mechanism | 5 | |
| OUTPAT | OUTPAT_ICD10(D829) | Immunodeficiency associated with major defect, unspecified | 5 | |
| OUTPAT | OUTPAT_ICD10(D8414) | C1 esterase inhibitor deficiency (C1-INH deficiency) | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D824) | Hyperimmunoglobulin E [IgE] syndrome. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D84) | Other immunodeficiencies. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D841) | Defects in the complement system. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8411) | Hereditary angioedema type I. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| PRIM_OUT | PRIM_OUT_NOT_USED_ICD10(D8989) | Other specified disorders involving the immune mechanism, not elsewhere classified. Not used in endpoint definition. POSSIBLY INACCURATE IN COMPLEX ENDPOINTS! | 5 | |
| REIMB | REIMB_KELA(132)_ICD10(D869) | Sarcoidosis, Sarcoidosis, unspecified | 5 |