Human Phenotype
Ontology
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Grandparent Node: Abnormality of the lymph nodes (HP:0002733) | Parent Node: Lymphadenopathy (HP:0002716) | ..Starting node ..Follicular hyperplasia (HP:0002729)
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Term ID: |
2729 |
Name: |
Follicular hyperplasia |
Synonym: |
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Definition: |
Lymphadenopathy (enlargement of lymph nodes) owing to hyperplasia of follicular (germinal) centers. |
Comments: |
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Reference: |
HP:0002729 |
Genes and Diseases: | | Child Nodes: | Sister Nodes: | ..Cervical lymphadenopathy (HP:0025289)
| ..Chronic noninfectious lymphadenopathy (HP:0002730)
| ..Generalized lymphadenopathy (HP:0008940)
| ..Mediastinal lymphadenopathy (HP:0100721)
| Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: | HPO disease - gene - phenotype less frequent non-typical associations: | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | CASP10 CL E G H | 843 | 1500 | OMIM:603909 | Autoimmune lymphoproliferative syndrome, type IIA | . | | | 87 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | CD19 CL E G H | 930 | 1633 | OMIM:240500 | Immunodeficiency, common variable, 2 | . | | | 38 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | CR2 CL E G H | 1380 | 2336 | OMIM:240500 | Immunodeficiency, common variable, 2 | . | | | 10 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | CTNNBL1 CL E G H | 56259 | 15879 | OMIM:619846 | | | | | | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | FAS CL E G H | 355 | 11920 | OMIM:601859 | Autoimmune lymphoproliferative syndrome | . | | | 59 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | FASLG CL E G H | 356 | 11936 | OMIM:601859 | Autoimmune lymphoproliferative syndrome | . | | | 37 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | ICOS CL E G H | 29851 | 5351 | OMIM:240500 | Immunodeficiency, common variable, 2 | . | | | 32 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | KRAS CL E G H | 3845 | 6407 | OMIM:614470 | RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic | . | | | 196 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | NRAS CL E G H | 4893 | 7989 | OMIM:614470 | RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic | . | | | 102 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | PRKCD CL E G H | 5580 | 9399 | OMIM:615559 | AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS3 | | | | 10 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | STING1 CL E G H | 340061 | 27962 | OMIM:615934 | STING-associated vasculopathy, infantile-onset | | | | | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | SYK CL E G H | 6850 | 11491 | OMIM:619381 | IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION; IMD82 | | | | 1 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | TET2 CL E G H | 54790 | 25941 | OMIM:619126 | IMMUNODEFICIENCY 75; IMD75 | | | | 3 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | TNFRSF13B CL E G H | 23495 | 18153 | OMIM:240500 | Immunodeficiency, common variable, 2 | . | | | 32 | | | HP:0002729 | HP:0002729 | Follicular hyperplasia | 0 | TNFRSF13C CL E G H | 115650 | 17755 | OMIM:240500 | Immunodeficiency, common variable, 2 | . | | | 12 | | |
Genes (15) :CASP10 CD19 CR2 CTNNBL1 FAS FASLG ICOS KRAS NRAS PRKCD STING1 SYK TET2 TNFRSF13B TNFRSF13C
Diseases (9) :OMIM:603909 OMIM:240500 OMIM:619846 OMIM:601859 OMIM:614470 OMIM:615559 OMIM:615934 OMIM:619381 OMIM:619126 |
Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.
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