Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the lymphatic system (HP:0100763)help
Parent Node:
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Abnormality of the lymph nodes (HP:0002733)help
..Starting node
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Lymph node hypoplasia (HP:0002732)help
Term ID: 2732
Name: Lymph node hypoplasia
Synonym: Small lymph nodes
Definition: Underdevelopment of the lymph nodes.
Comments:
Reference: HP:0002732
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of mesenteric lymph nodes (HP:0025042) help
..expandAbsence of lymph node germinal center (HP:0002849) help
..expandLymphadenitis (HP:0002840) help
..expandLymphadenopathy (HP:0002716) 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:0002732HP:0002732Lymph node hypoplasia0BTK CL E G H6951133OMIM:300755Agammaglobulinemia, X-linked.109
HP:0002732HP:0002732Lymph node hypoplasia0DCLRE1C CL E G H6442117642OMIM:602450Severe combined immunodeficiency with sensitivity to ionizing radiation.94
HP:0002732HP:0002732Lymph node hypoplasia0EPHB4 CL E G H20503395ORPHA:90186Meige diseaseHP:0040282 - Frequent3
HP:0002732HP:0002732Lymph node hypoplasia0IL2RG CL E G H35616010ORPHA:276T-B+ severe combined immunodeficiency due to gamma chain deficiencyHP:0040283 - Occasional48
HP:0002732HP:0002732Lymph node hypoplasia0PNP CL E G H48607892OMIM:613179Immunodeficiency due to purine nucleoside phosphorylase deficiency.52


Genes (5) :BTK DCLRE1C EPHB4 IL2RG PNP

Diseases (5) :OMIM:300755 OMIM:602450 ORPHA:90186 ORPHA:276 OMIM:613179
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.