DiseaseID 14647
淋巴增殖性疾病
disease
NCI2016_02D:An X-linked immunodeficiency syndrome that exclusivesly affects males, although females can be carriers. The syndrome is characterized by life-threatening episodes of infectious mononucleosis, hypogammaglobul
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Disease: 1Herb: 12Symptom: 12Target: 24Links: 48
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14647
- Core Entity Id
- 72462
- Source Entity Count
- 1
- Preferred Name
- Lymphoproliferative Disorders
- Name Cn
- 淋巴增殖性疾病
- Name Pinyin
- Lin Ba Zeng Zhi Xing Ji Bing
- Name En
- Lymphoproliferative Disorders
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesInfections; Pathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entitydisease of anatomical entity; genetic diseasedisease of anatomical entity; genetic disease; disease of cellular proliferation
- Hpo Class
- Abnormality of blood and blood-forming tissues; Neoplasm
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Infections
- Hpo Class Name
- Neoplasm; Abnormality of blood and blood-forming tissues
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entitygenetic disease; disease of anatomical entity; disease of cellular proliferation
- Disease Definition
- NCI2016_02D:An X-linked immunodeficiency syndrome that exclusivesly affects males, although females can be carriers. The syndrome is characterized by life-threatening episodes of infectious mononucleosis, hypogammaglobulinemia, and subsequent development of lymphomas (usually B-cell lymphomas) and other lymphoproliferative disorders.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Lymphoproliferative Disorders
Role
preferred
Name
Autoimmune Lymphoproliferative Syndrome
Role
preferred
Name
Autoimmune Lymphoproliferative Syndrome, Type Iia
Role
preferred
Name
Autoimmune Lymphoproliferative Syndrome, Type Iii
Role
preferred
Name
Lymphoproliferative Syndrome 1
Role
preferred
Name
Lymphoproliferative Syndrome 2
Role
preferred
Name
Lymphoproliferative Syndrome, X-Linked, 2
Role
preferred
Name
Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Role
preferred
Name
Autoimmune Lymphoproliferative Syndrome Type 2B
Role
preferred
Name
Autoimmune Lymphoproliferative Syndrome, Type IA
Role
preferred
Name
Autoimmune Lymphoproliferative Syndrome, Type IB
Role
preferred
Name
Immunodeficiency Following Hereditary Defective Response To Epstein-Barr Virus
Role
preferred
Name
Lymphoproliferative Syndrome, X-Linked, 1
Role
preferred
Name
Neoplasm of Uncertain Behavior of Lymphoid, Hematopoietic And Related Tissue, Unspecified
Role
preferred
Name
X-Linked Lymphoproliferative Disorder
Role
preferred
Name
ALPS
Role
alias
Name
ALPS1A
Role
alias
Name
ALPS1B
Role
alias
Name
ALPS2
Role
alias
Name
ALPS2A
Role
alias
Name
ALPS3
Role
alias
Name
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL DOMINANT
Role
alias
Name
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE I, AUTOSOMAL RECESSIVE
Role
alias
Name
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE II
Role
alias
Name
Autoimmune Lymphoproliferative Syndrome Type 2A
Role
alias
Name
Autoimmune Lymphoproliferative Syndrome Type 3
Role
alias
Name
CANALE-SMITH SYNDROME
Role
alias
Name
CD27 DEFICIENCY
Role
alias
Name
CVID9, FORMERLY
Role
alias
Name
Caspase 8 Deficiency
Role
alias
Name
Ceds
Role
alias
Name
Ebvs
Role
alias
Name
IMMUNODEFICIENCY, COMMON VARIABLE, 9, FORMERLY
Role
alias
Name
LPFS1
Role
alias
Name
LPFS2
Role
alias
Name
Lymphoproliferative Disorder
Role
alias
Name
Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood
Role
alias
Name
X-Linked Lymphoproliferative Syndrome 1
Role
alias
Name
X-Linked Lymphoproliferative Syndrome 2
Role
alias
Name
XIAP DEFICIENCY
Role
alias
Name
XLP2
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0005523
Herb
HBDIS001819HBDIS009501HBDIS010136HBDIS013562HBDIS016176HBDIS016335HBDIS017593HBDIS018279HBDIS018280HBDIS019677HBDIS020055HBDIS021733HBDIS021869HBDIS022391
Me Sh
D008232D056735
Omim
300635308240601859603909607271613011615122615559
Umls
C0024314C0549463C1328840C1845076C1858968C1866119C1866120C1866121C3552634C3554540C3809928
Icd10
D47.9D82.3
Med Dra
10068348
Sym Map
SMDE00031SMDE00503SMDE00660SMDE01073SMDE01165SMDE02054SMDE04867SMDE10617
Do Class
DOID:14566DOID:630DOID:7
Dis Ge Net
C0024314C0451697C0549463C1328840C1845076C1846545C1858968C1866119C1866120C2717884C2873719C3552634C3554540C3809928
Orphanet
2442
Umls Sty
T047T191
Hpo Class
HP:0001871HP:0002664
Me Sh Class
C01C15C16C20C23
Etcm Disease
Autoimmune Lymphoproliferative SyndromeAutoimmune Lymphoproliferative Syndrome, Type IiaLymphoproliferative Syndrome 1Lymphoproliferative Syndrome 2Lymphoproliferative Syndrome, X-Linked, 1Lymphoproliferative Syndrome, X-Linked, 2
Tcmbank Disease
101691264814544184631930831982322384286441556616858873990209203
Itcmdb Generated
ITX-DISEASE-3F9BCC131C63ITX-DISEASE-470CA82ED936ITX-DISEASE-95BAC43877E0ITX-DISEASE-A064DF1986B5ITX-DISEASE-A48D7CA676EBITX-DISEASE-DDB08059E504ITX-DISEASE-E1DDA9E8387FITX-DISEASE-FA7DCF915DD8
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Page Title
Disease Autoimmune Lymphoproliferative Syndrome Details pageDisease Autoimmune Lymphoproliferative Syndrome, Type Iia Details pageDisease Lymphoproliferative Syndrome 1 Details pageDisease Lymphoproliferative Syndrome 2 Details pageDisease Lymphoproliferative Syndrome, X-Linked, 1 Details pageDisease Lymphoproliferative Syndrome, X-Linked, 2 Details page
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entitygenetic disease; disease of anatomical entity; disease of cellular proliferation
Disease Type
diseasegroupphenotype
Hpo Class Name
Neoplasm; Abnormality of blood and blood-forming tissues
Do Disease Class
disease of anatomical entitydisease of anatomical entity; genetic diseasedisease of anatomical entity; genetic disease; disease of cellular proliferation
Hpo Disease Class
Abnormality of blood and blood-forming tissues; Neoplasm
Umls Disease Type
Disease or SyndromeNeoplastic Process
Basic Information
Disease Name
Autoimmune Lymphoproliferative Syndrome
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Gastrointestinal Diseases;Immune diseases
Disease Name
Autoimmune Lymphoproliferative Syndrome, Type Iia
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Gastrointestinal Diseases;Immune diseases
Disease Name
Lymphoproliferative Syndrome 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Gastrointestinal Diseases;Immune diseases
Disease Name
Lymphoproliferative Syndrome 2
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Gastrointestinal Diseases;Immune diseases
Disease Name
Lymphoproliferative Syndrome, X-Linked, 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Name
Lymphoproliferative Syndrome, X-Linked, 2
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Immune diseases
Disease Definition
NCI2016_02D:An X-linked immunodeficiency syndrome that exclusivesly affects males, although females can be carriers. The syndrome is characterized by life-threatening episodes of infectious mononucleosis, hypogammaglobulinemia, and subsequent development of lymphomas (usually B-cell lymphomas) and other lymphoproliferative disorders.NCI2016_02D:An autoimmune hematologic disorder characterized by autoimmune hemolytic anemia, thrombocytopenia, lymphadenopathy, hepatomegaly and splenomegaly. Patients are at an increased risk of developing Hodgkin and non-Hodgkin lymphomas.|MSH2017_2016_08_12:Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.NCI2016_NCI-GLOSS_1602D:A disease in which cells of the lymphatic system grow excessively. Lymphoproliferative disorders are often treated like cancer.|NCI2016_02D:A disorder characterized by proliferation of lymphocytes at various stages of differentiation. Lymphoproliferative disorders can be neoplastic (clonal, as in lymphomas and leukemias) or reactive (polyclonal, as in infectious mononucleosis).|MSH2017_2016_08_12:Disorders characterized by proliferation of lymphoid tissue, general or unspecified.
Me Sh Disease Class
Immune System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesInfections; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasegroupphenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic DiseasesImmune System Diseases; Hemic and Lymphatic DiseasesPathological Conditions, Signs and Symptoms; Infections
Umls Semantic Type Name
Disease or SyndromeNeoplastic Process