ValueSet-2.16.840.1.114222.4.11.3060

Include these codes as defined in http://snomed.info/sct version http://snomed.info/sct/731000124108/version/20200901

Code	Display
234640004	18-p syndrome with associated immunodeficiency (disorder)
719685004	Absent thumb with short stature and immunodeficiency syndrome (disorder)
62479008	Acquired immune deficiency syndrome (disorder)
10746341000119109	Acquired immune deficiency syndrome complicating childbirth (disorder)
735434003	Acquired neutrophilia (disorder)
711480000	Activated PI3K-delta syndrome (disorder)
47144000	Acute neutrophilia (disorder)
44940001	Adenosine deaminase deficiency (disorder)
735536003	Adult-onset immunodeficiency (disorder)
722281001	Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder)
234642007	Age-related immunodeficiency (disorder)
17182001	Agranulocytosis (disorder)
421312009	Agranulocytosis associated with acquired immunodeficiency syndrome (disorder)
713530002	Agranulocytosis co-occurrent with human immunodeficiency virus infection (disorder)
14333004	Alloimmune neonatal neutropenia (disorder)
234604001	Alternative pathway deficiency (disorder)
234627009	Anaphylotoxin inactivator deficiency (disorder)
703525006	Anhidrotic ectodermal dysplasia with immune deficiency (disorder)
720986005	Anhidrotic ectodermal dysplasia, immunodeficiency, osteopetrosis, lymphedema syndrome (disorder)
234558001	Anti-haemophilus influenzae B polysaccharide antibody deficiency (disorder)
234560004	Anti-meningococcal polysaccharide A antibody deficiency (disorder)
234561000	Anti-meningococcal polysaccharide C antibody deficiency (disorder)
234559009	Anti-pneumococcal polysaccharide antibody deficiency (disorder)
234557006	Anti-polysaccharide antibody deficiency (disorder)
234562007	Anti-protein antibody deficiency (disorder)
234563002	Anti-staphylococcal antibody deficiency (disorder)
24181002	Aplasia of thymus gland with immunodeficiency (disorder)
68504005	Ataxia-telangiectasia syndrome (disorder)
720520009	Attenuated Ch+Â¬diak-Higashi syndrome (disorder)
722288007	Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder)
722290008	Autoimmune lymphoproliferative syndrome with recurrent viral infection (disorder)
234425008	Autoimmune neutropenia (disorder)
234534000	Autosomal agammaglobulinemia with absent B-cells (disorder)
725150008	Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)
725151007	Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)
770947009	Autosomal dominant severe congenital neutropenia (disorder)
403836001	Autosomal recessive hyperimmunoglobulin M syndrome (disorder)
771309000	Autosomal recessive lymphoproliferative disease (disorder)
725431001	Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency (disorder)
725432008	Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency (disorder)
190993005	Autosomal recessive severe combined immunodeficiency (disorder)
362993009	Autosomal recessive severe combined immunodeficiency disease (disorder)
234572005	Benign combined immunodeficiency (disorder)
129640007	Benign granulocytopenia in childhood (disorder)
4434006	Bloom syndrome (disorder)
402791005	B-lymphocyte immunodeficiency (disorder)
234633000	Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency (disorder)
111396008	Ch+Â¬diak-Higashi syndrome (disorder)
276628009	Chloramphenicol-induced neutropenia (disorder)
234634006	Chromosome 18 syndromes and antibody deficiency (disorder)
234635007	Chromosome 22 abnormalities with hypogammaglobulinemia (disorder)
234418001	Chronic benign granulocytopenia (disorder)
234423001	Chronic benign neutropenia (disorder)
129641006	Chronic benign neutropenia of childhood (disorder)
234576008	Chronic familial neutropaenia (disorder)
387759001	Chronic granulomatous disease (disorder)
29272001	Chronic granulomatous disease, type I (disorder)
40197009	Chronic granulomatous disease, type IA (disorder)
77330006	Chronic granulomatous disease, type II (disorder)
26252007	Chronic granulomatous disease, type IIA (disorder)
82317007	Chronic granulomatous disease, type III (disorder)
21527007	Chronic granulomatous disease, type IV (disorder)
76243000	Chronic granulomatous disease, type IVA (disorder)
129643009	Chronic hypoplastic neutropenia (disorder)
129642004	Chronic idiopathic immunoneutropenia in adults (disorder)
248693006	Chronic idiopathic neutropenia (disorder)
80369006	Chronic neutrophilia (disorder)
234593008	Classical complement pathway abnormality (disorder)
234613004	Combined complement 6 and 7 deficiencies (disorder)
442459007	Combined immunodeficiency disease (disorder)
717811007	Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder)
725135004	Combined immunodeficiency due to CD3gamma deficiency (disorder)
773488000	Combined immunodeficiency due to mucosa-associated lymphoid tissue lymphoma translocation gene 1 deficiency (disorder)
766879006	Combined immunodeficiency due to OX40 deficiency (disorder)
725290000	Combined immunodeficiency due to partial recombination-activating gene 1 deficiency (disorder)
771479000	Combined immunodeficiency due to serine/threonine kinase 4 deficiency (disorder)
716378008	Combined immunodeficiency due to Zeta-chain associated protein kinase 70 deficiency (disorder)
770625006	Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder)
234547005	Combined immunoglobulin G2 and G4 deficiency (disorder)
234591005	Combined phagocytic defect (disorder)
23238000	Common variable agammaglobulinemia (disorder)
191013002	Common variable immunodeficiency with autoantibodies to B- or T-cells (disorder)
191011000	Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions (disorder)
191012007	Common variable immunodeficiency with predominant immunoregulatory T-cell disorders (disorder)
234595001	Complement 1q beta chain deficiency (disorder)
234594002	Complement 1q deficiency (disorder)
234596000	Complement 1q dysfunction (disorder)
234597009	Complement 1r deficiency (disorder)
234598004	Complement 1s deficiency (disorder)
234599007	Complement 2 deficiency (disorder)
234603007	Complement 3 deficiency (disorder)
234623008	Complement 4 binding protein deficiency (disorder)
234600005	Complement 4 deficiency (disorder)
234601009	Complement 4A deficiency (disorder)
234602002	Complement 4B deficiency (disorder)
234609006	Complement 5 deficiency (disorder)
263661007	Complement 5 dysfunction (disorder)
234626000	Complement 5a inhibitor deficiency (disorder)
234611002	Complement 6 deficiency (disorder)
234612009	Complement 7 deficiency (disorder)
234616007	Complement 8 alpha-gamma deficiency (disorder)
234614005	Complement 8 beta chain deficiency (disorder)
234615006	Complement 8 beta chain dysfunction (disorder)
234617003	Complement 9 deficiency (disorder)
18827005	Complement abnormality (disorder)
771443008	Complement component 3 deficiency (disorder)
363009005	Complement component deficiency (disorder)
24743004	Complement deficiency disease (disorder)
234629007	Complement receptor 1 deficiency (disorder)
234630002	Complement receptor 3 deficiency (disorder)
234628004	Complement receptor deficiency (disorder)
234618008	Complement regulatory factor defect (disorder)
116133005	Congenital agammaglobulinemia (disorder)
58034007	Congenital hypergammaglobulinemia (disorder)
36138009	Congenital immunodeficiency disease (disorder)
363040003	Congenital immunodeficiency involving the hematopoietic system (disorder)
77358003	Congenital leukocyte adherence deficiency (disorder)
89655007	Congenital neutropenia (disorder)
775909002	Congenital neutropenia, myelofibrosis, nephromegaly syndrome (disorder)
765327005	Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (disorder)
764946008	Constitutional mismatch repair deficiency syndrome (disorder)
735435002	Constitutional neutrophilia (disorder)
234426009	Corticosteroid-induced neutrophilia (disorder)
191347008	Cyclical neutropenia (disorder)
350353007	De Vaal's syndrome (disorder)
234624002	Decay accelerating factor deficiency (disorder)
234555003	Defective immunoglobulin glycosylation (disorder)
234581004	Defective phagocytic cell adhesion (disorder)
234580003	Defective phagocytic cell chemotaxis (disorder)
234585008	Defective phagocytic cell killing (disorder)
234578009	Defective phagocytic cell opsonization (disorder)
773664005	Deficiency in anterior pituitary function, variable immunodeficiency syndrome (disorder)
234637004	Deletion of X-chromosome and hypogammaglobulinemia (disorder)
24419001	Disorder of complement (disorder)
234574006	Disorder of phagocytic cell number (disorder)
56918001	Dose-related drug-induced neutropenia (disorder)
234645009	Drug-induced immunodeficiency (disorder)
47318007	Drug-induced neutropenia (disorder)
63484008	Drug-induced neutrophilia (disorder)
48119005	Dysplasia of thymus gland with immunodeficiency (disorder)
771515001	Facial dysmorphism, immunodeficiency, livedo, short stature syndrome (disorder)
234605000	Factor B deficiency (disorder)
234607008	Factor D deficiency (disorder)
234622003	Factor H deficiency (disorder)
234621005	Factor I deficiency (disorder)
39674000	Familial C3B inhibitor deficiency syndrome (disorder)
699861000	Familial granulomatous inflammatory arthritis, dermatitis and uveitis (disorder)
398250003	Familial hemophagocytic lymphohistiocytosis (disorder)
234566005	Familial immunoglobulin hypercatabolism (disorder)
247860002	Familial neutropenia (disorder)
426800001	Febrile granulocytopenia (disorder)
409089005	Febrile neutropenia (disorder)
267543009	Functional disorders of polymorphonuclear neutrophils (disorder)
234590006	Gluthathione peroxidase deficiency (disorder)
234589002	Gluthathione synthetase deficiency (disorder)
417672002	Granulocytopenic disorder (disorder)
234436001	Hemolytic erythrophagocytic syndrome (disorder)
234437005	Hemophagocytic lymphohistiocytosis (disorder)
713444005	Hemophagocytic syndrome co-occurrent with human immunodeficiency virus infection (disorder)
190959006	Hemophagocytic syndrome, infection-associated (disorder)
724361001	Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder)
82966003	Hereditary angioedema (disorder)
427167008	Hereditary angioedema with normal C1 esterase inhibitor activity (disorder)
234619000	Hereditary C1 esterase inhibitor deficiency - deficient factor (disorder)
234620006	Hereditary C1 esterase inhibitor deficiency - dysfunctional factor (disorder)
129639005	Hereditary neutrophilia (finding)
234625001	Homologous restriction factor deficiency (disorder)
82286005	Hyperimmunoglobulin M syndrome (disorder)
37548006	Hypopigmentation-immunodeficiency disease (disorder)
763713000	Idiopathic CD4 lymphocytopenia (disorder)
771333006	Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection syndrome (disorder)
65623009	Immune neutropenia (disorder)
234632005	Immunodeficiency associated with chromosomal abnormality (disorder)
234641000	Immunodeficiency associated with multiple organ system abnormalities (disorder)
725136003	Immunodeficiency by defective expression of human leukocyte antigen class 1 (disorder)
103079001	Immunodeficiency caused by corticosteroid (disorder)
10838971000119103	Immunodeficiency caused by long term therapeutic use of drug (disorder)
234532001	Immunodeficiency disorder (disorder)
778028008	Immunodeficiency due to CD25 deficiency (disorder)
766705006	Immunodeficiency due to ficolin 3 deficiency (disorder)
771078002	Immunodeficiency due to mannan binding lectin serine peptidase 2 deficiency (disorder)
723334006	Immunodeficiency due to mutation of FAS-associated protein with death domain gene (disorder)
191008001	Immunodeficiency following hereditary defective response to Epstein-Barr virus (disorder)
103081004	Immunodeficiency secondary to chemotherapy (disorder)
103077004	Immunodeficiency secondary to neoplasm (disorder)
103080003	Immunodeficiency secondary to radiation therapy (disorder)
103078009	Immunodeficiency secondary to trauma (disorder)
234631003	Immunodeficiency with major anomalies (disorder)
402483002	Immunodeficiency with multicarboxylase deficiency (disorder)
9893005	Immunodeficiency with thymoma (disorder)
29260007	Immunoglobulin A deficiency (disorder)
234551007	Immunoglobulin A1 deficiency (disorder)
234552000	Immunoglobulin A2 deficiency (disorder)
417167007	Immunoglobulin deficiency (disorder)
12631000119106	Immunoglobulin G deficiency (disorder)
234550008	Immunoglobulin G1 deficiency (disorder)
234546001	Immunoglobulin G2 deficiency (disorder)
234548000	Immunoglobulin G3 deficiency (disorder)
234549008	Immunoglobulin G4 deficiency (disorder)
234539005	Immunoglobulin heavy chain deficiency (disorder)
234565009	Immunoglobulin hypercatabolism (disorder)
234543009	Immunoglobulin light chain deficiency (disorder)
234544003	Immunoglobulin subclass deficiency (disorder)
234553005	Immunoglobulin-associated molecule deficiency (disorder)
7990002	Immunoglobulinemia with isolated somatotropin deficiency (disorder)
254067002	Immuno-osseous dysplasia (disorder)
449853003	Interleukin-12 deficiency (disorder)
78378009	Isoimmune neutropenia (disorder)
764858009	Isolated agammaglobulinemia (disorder)
50926003	Job's syndrome (disorder)
449187006	Kappa light chain deficiency (disorder)
770942003	Kostmann syndrome (disorder)
449384005	Lambda light chain deficiency (disorder)
724179008	Laron syndrome with immunodeficiency (disorder)
71436005	Lazy leukocyte syndrome (disorder)
234582006	Leukocyte adhesion deficiency - type 1 (disorder)
234583001	Leukocyte adhesion deficiency - type 2 (disorder)
234586009	Leukocyte glucose-6-phosphate dehydrogenase deficiency (disorder)
763668009	Lichtenstein syndrome (disorder)
724177005	Ligase 4 syndrome (disorder)
234577004	Lipochrome histiocytosis - familial (disorder)
721977007	Lung fibrosis, immunodeficiency, 46,XX gonadal dysgenesis syndrome (disorder)
191018006	Lymphocyte function antigen-1 defect (disorder)
25109007	Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome (disorder)
771073006	Lymphoproliferative disorder caused by methotrexate (disorder)
430478003	Macrophage activation syndrome (disorder)
191001007	Major histocompatibility complex class I deficiency (disorder)
191002000	Major histocompatibility complex class II deficiency (disorder)
234579001	Mannan-binding protein deficiency (disorder)
703538003	Mannose-binding lectin deficiency (disorder)
80255009	Maternal transfer neutropenia (disorder)
768560008	Melanoma differentiation-associated gene 5 deficiency (disorder)
718230004	Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 1 deficiency (disorder)
721876004	Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency (disorder)
723384004	Mendelian susceptibility to mycobacterial disease due to complete interferon stimulated gene 15 deficiency (disorder)
716869006	Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 receptor beta 1 deficiency (disorder)
721877008	Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency (disorder)
723385003	Mendelian susceptibility to mycobacterial disease due to partial interferon regulatory factor 8 deficiency (disorder)
723386002	Mendelian susceptibility to mycobacterial disease due to partial signal transducer and activator of transcription 1 deficiency (disorder)
234424007	Metabolic neutropenia (disorder)
304576008	Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency (disorder)
721903007	Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder)
234638009	Microcephaly, normal intelligence and immunodeficiency (disorder)
778024005	Monocytopenia with susceptibility to infections (disorder)
234636008	Monosomy 22 and absence of immunoglobulin A (disorder)
24974008	Myelokathexis (disorder)
234433009	Myeloperoxidase deficiency (disorder)
737307003	Natural-killer cell deficiency (disorder)
773662009	Neonatal inflammatory skin and bowel disease (disorder)
416729007	Neutropenia associated with AIDS (disorder)
111585004	Neutropenia associated with autoimmune disease (disorder)
46359005	Neutropenia associated with infectious disease (disorder)
767658000	Neutropenia due to and following chemotherapy (disorder)
267540007	Neutropenia due to irradiation (disorder)
276576000	Neutropenia of the small for gestational age baby (disorder)
41814009	Neutropenia with dysgranulopoiesis (disorder)
725137007	Neutropenia, monocytopenia, deafness syndrome (disorder)
303011007	Neutropenic disorder (disorder)
723443003	Neutrophil immunodeficiency syndrome (disorder)
234587000	Neutrophil lactoferrin deficiency (disorder)
234588005	Neutrophil secondary granule deficiency (disorder)
414850009	Neutrophilia (disorder)
71610005	Neutrophilic leukemoid reaction (disorder)
55602000	Nezelof's syndrome (disorder)
3902000	Non dose-related drug-induced neutropenia (disorder)
773730002	Osteopetrosis hypogammaglobulinemia syndrome (disorder)
709608008	Periodontitis co-occurrent with acquired neutropenia (disorder)
709465004	Periodontitis co-occurrent with Ch+Â¬diak-Higashi syndrome (disorder)
710927004	Periodontitis co-occurrent with cyclical neutropenia (disorder)
710926008	Periodontitis co-occurrent with familial neutropenia (disorder)
709535007	Periodontitis co-occurrent with infantile genetic agranulocytosis (disorder)
710735009	Periodontitis co-occurrent with leukocyte adhesion deficiency (disorder)
234573000	Phagocytic cell defect (disorder)
302874002	Phagocytic cell dysfunction (disorder)
707152007	Phagocytic immunodeficiency (disorder)
773646003	Phospholipase C gamma 2 associated antibody deficiency and immune dysregulation (disorder)
772126000	Poikiloderma with neutropenia (disorder)
778027003	Primary CD59 deficiency (disorder)
58606001	Primary immune deficiency disorder (disorder)
718717004	Primary immunodeficiency syndrome due to p14 deficiency (disorder)
724275005	Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder)
234564008	Primary immunoglobulin catabolism abnormality (disorder)
191338000	Primary splenic neutropenia (disorder)
81166004	Properdin deficiency disease (disorder)
70349007	Pseudoneutrophilia (disorder)
60743005	Purine-nucleoside phosphorylase deficiency (disorder)
724015007	Pyogenic arthritis, pyoderma gangrenosum, acne syndrome (disorder)
718232007	Pyogenic bacterial infection due to deficiency of myeloid differentiation primary response 88 (disorder)
105602005	Quantitative abnormality of granulocytes (disorder)
105601003	Quantitative disorder of neutrophils (disorder)
723508002	RAS-associated autoimmune leukoproliferative disease (disorder)
111584000	Reticular dysgenesis (disorder)
351287008	Reticular dysgenesis with congenital aleukocytosis (disorder)
773404000	Roifman syndrome (disorder)
723995003	Schimke immuno-osseous dysplasia (disorder)
36980009	SCID due to absent adenosine deaminase (disorder)
71904008	SCID due to absent class II HLA antigens (disorder)
111587007	SCID due to absent IL-2 receptor (disorder)
3439009	SCID due to absent peripheral T cell maturation (disorder)
49555001	SCID due to absent T cell receptor (disorder)
33286000	Secondary immune deficiency disorder (disorder)
234554004	Secretory piece deficiency (disorder)
190979003	Selective immunoglobulin A deficiency (disorder)
234541006	Selective immunoglobulin D deficiency (disorder)
234540007	Selective immunoglobulin E deficiency (disorder)
190981001	Selective immunoglobulin G deficiency (disorder)
234542004	Selective immunoglobulin M and immunoglobulin A deficiency (disorder)
190980000	Selective immunoglobulin M deficiency (disorder)
31323000	Severe combined immunodeficiency disease (disorder)
45390000	Severe combined immunodeficiency due to absent interleukin-2 production (disorder)
22406001	Severe combined immunodeficiency due to absent lymphoid stem cells (disorder)
771517009	Severe combined immunodeficiency due to caspase recruitment domain family member 11 deficiency (disorder)
765188009	Severe combined immunodeficiency due to complete recombination-activating gene 1 and/or recombination-activating gene 2 deficiency (disorder)
763623001	Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency (disorder)
715982006	Severe combined immunodeficiency due to deoxyribonucleic acid cross-link repair protein 1c deficiency (disorder)
716871006	Severe combined immunodeficiency due to deoxyribonucleic acid dependent protein kinase catalytic subunit deficiency (disorder)
718107000	Severe combined immunodeficiency T-cell negative B-cell positive due to janus kinase-3 deficiency (disorder)
722067005	Severe combined immunodeficiency with hypereosinophilia (disorder)
190998001	Severe combined immunodeficiency with low or normal B-cell numbers (disorder)
190997006	Severe combined immunodeficiency with low T- and B-cell numbers (disorder)
234570002	Severe combined immunodeficiency with maternofetal engraftment (disorder)
720853005	Severe combined immunodeficiency, microcephaly, growth retardation, sensitivity to ionizing radiation syndrome (disorder)
190996002	Severe combined immunodefiency with reticular dysgenesis (disorder)
774211005	Severe dermatitis, multiple allergies, metabolic wasting syndrome (disorder)
720345008	Severe T-cell immunodeficiency, congenital alopecia, nail dystrophy syndrome (disorder)
89454001	Shwachman syndrome (disorder)
234556002	Specific antibody deficiency (disorder)
726078000	Sporadic Blau syndrome (disorder)
773702002	Sterile multifocal osteomyelitis with periostitis and pustulosis (disorder)
127067009	Stress neutrophilia (finding)
766983005	Susceptibility to respiratory infection associated with CD8alpha chain mutation (disorder)
778045003	Susceptibility to viral and mycobacterial infection (disorder)
778023004	Syndromic multisystem autoimmune disease due to itchy E3 ubiquitin protein ligase deficiency (disorder)
765145001	T cell negative B cell positive severe combined immunodeficiency due to gamma chain deficiency (disorder)
770785002	T-cell immunodeficiency due to ras homolog family member H deficiency (disorder)
234608003	Terminal component deficiency (disorder)
190995003	Thymic aplasia or dysplasia with immunodeficiency (disorder)
402792003	T-lymphocyte immunodeficiency (disorder)
32092008	Toxic neutropenia (disorder)
88714009	Transient hypogammaglobulinemia of infancy (disorder)
234643002	Transient immunodeficiency of infancy (disorder)
55444004	Transient neonatal neutropenia (disorder)
234639001	Triple X syndrome, epilepsy, and hypogammaglobulinemia (disorder)
234584007	Tuftsin deficiency (disorder)
770687001	Vasculitis due to adenosine deaminase 2 deficiency (disorder)
719824001	Vici syndrome (disorder)
234571003	Warts, hypogammaglobulinemia, infections, and myelokathexis (disorder)
403837005	Wiskott-Aldrich autosomal dominant variant syndrome (disorder)
36070007	Wiskott-Aldrich syndrome (disorder)
65880007	X-linked agammaglobulinemia (disorder)
234533006	X-linked agammaglobulinemia with growth hormone deficiency (disorder)
403835002	X-linked hyper-immunoglobulin M syndrome (disorder)
234416002	X-linked hypogammaglobulinemia (disorder)
724276006	X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder)
719827008	X-linked immunoneurologic disorder (disorder)
719156006	X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder)
77121009	X-linked lymphoproliferative syndrome (disorder)
719814009	X-linked mendelian susceptibility to mycobacterial disease (disorder)
718882006	X-linked severe congenital neutropenia (disorder)