Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the lymph nodes (HP:0002733)help
Parent Node:
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Lymphadenopathy (HP:0002716)help
..Starting node
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Follicular hyperplasia (HP:0002729)help
Term ID: 2729
Name: Follicular hyperplasia
Synonym:
Definition: Lymphadenopathy (enlargement of lymph nodes) owing to hyperplasia of follicular (germinal) centers.
Comments:
Reference: HP:0002729
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCervical lymphadenopathy (HP:0025289) help
..expandChronic noninfectious lymphadenopathy (HP:0002730) help
..expandGeneralized lymphadenopathy (HP:0008940) help
..expandMediastinal lymphadenopathy (HP:0100721) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0002729HP:0002729Follicular hyperplasia0CASP10 CL E G H8431500OMIM:603909Autoimmune lymphoproliferative syndrome, type IIA.87
HP:0002729HP:0002729Follicular hyperplasia0CD19 CL E G H9301633OMIM:240500Immunodeficiency, common variable, 2.38
HP:0002729HP:0002729Follicular hyperplasia0CR2 CL E G H13802336OMIM:240500Immunodeficiency, common variable, 2.10
HP:0002729HP:0002729Follicular hyperplasia0CTNNBL1 CL E G H5625915879OMIM:619846
HP:0002729HP:0002729Follicular hyperplasia0FAS CL E G H35511920OMIM:601859Autoimmune lymphoproliferative syndrome.59
HP:0002729HP:0002729Follicular hyperplasia0FASLG CL E G H35611936OMIM:601859Autoimmune lymphoproliferative syndrome.37
HP:0002729HP:0002729Follicular hyperplasia0ICOS CL E G H298515351OMIM:240500Immunodeficiency, common variable, 2.32
HP:0002729HP:0002729Follicular hyperplasia0KRAS CL E G H38456407OMIM:614470RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic.196
HP:0002729HP:0002729Follicular hyperplasia0NRAS CL E G H48937989OMIM:614470RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic.102
HP:0002729HP:0002729Follicular hyperplasia0PRKCD CL E G H55809399OMIM:615559AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III; ALPS310
HP:0002729HP:0002729Follicular hyperplasia0STING1 CL E G H34006127962OMIM:615934STING-associated vasculopathy, infantile-onset
HP:0002729HP:0002729Follicular hyperplasia0SYK CL E G H685011491OMIM:619381IMMUNODEFICIENCY 82 WITH SYSTEMIC INFLAMMATION; IMD821
HP:0002729HP:0002729Follicular hyperplasia0TET2 CL E G H5479025941OMIM:619126IMMUNODEFICIENCY 75; IMD753
HP:0002729HP:0002729Follicular hyperplasia0TNFRSF13B CL E G H2349518153OMIM:240500Immunodeficiency, common variable, 2.32
HP:0002729HP:0002729Follicular hyperplasia0TNFRSF13C CL E G H11565017755OMIM:240500Immunodeficiency, 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.