Human Phenotype Ontology 
Grandparent Node:
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Abnormal liver morphology (HP:0410042)help
Grandparent Node:
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Increased inflammatory response (HP:0012649)help
Parent Node:
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Hepatitis (HP:0012115)help
..Starting node
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Chronic hepatitis (HP:0200123)help
Term ID: 200123
Name: Chronic hepatitis
Synonym: Chronic liver inflammation
Definition: Hepatitis that lasts for more than six months.
Comments:
Reference: HP:0200123
Genes and Diseases:
 
       Child Nodes:
........expandChronic active hepatitis (HP:0200120) help
........expandChronic hepatitis due to cryptosporidium infection (HP:0200124) help

 Sister Nodes: 
..expandAcute hepatitis (HP:0200119) help
..expandAtypical or prolonged hepatitis (HP:0200122) help
..expandFulminant hepatitis (HP:0004787) help
..expandGiant cell hepatitis (HP:0200084) help
..expandViral hepatitis (HP:0006562) 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:0200123HP:0200123Chronic hepatitis0AIRE CL E G H326360OMIM:240300AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA; APS192
HP:0200123HP:0200123Chronic hepatitis0ALMS1 CL E G H7840428OMIM:203800Alstrom syndrome404
HP:0200123HP:0200123Chronic hepatitis0C4B CL E G H7211324OMIM:614379Complement component 4B deficiency1
HP:0200123HP:0200123Chronic hepatitis0CD40LG CL E G H95911935OMIM:308230Immunodeficiency, X-linked, with hyper-IgM.33
HP:0200123HP:0200123Chronic hepatitis0CIITA CL E G H42617067ORPHA:572Immunodeficiency by defective expression of MHC class II118
HP:0200123HP:0200123Chronic hepatitis0HBB CL E G H30434827ORPHA:231226Dominant beta-thalassemiaHP:0040283 - Occasional580
HP:0200123HP:0200123Chronic hepatitis0IL21R CL E G H506156006OMIM:615207IMMUNODEFICIENCY 56; IMD567
HP:0200123HP:0200123Chronic hepatitis0PGM1 CL E G H52368905OMIM:614921Congenital disorder of glycosylation, type It58
HP:0200123HP:0200123Chronic hepatitis0RFX5 CL E G H59939986ORPHA:572Immunodeficiency by defective expression of MHC class II38
HP:0200123HP:0200123Chronic hepatitis0RFXANK CL E G H86259987ORPHA:572Immunodeficiency by defective expression of MHC class II26
HP:0200123HP:0200123Chronic hepatitis0RFXAP CL E G H59949988ORPHA:572Immunodeficiency by defective expression of MHC class II34
HP:0200123HP:0200123Chronic hepatitis0SKIC2 CL E G H649910898OMIM:614602Trichohepatoenteric syndrome 2
HP:0200123HP:0200120Chronic active hepatitis1AIRE CL E G H326360OMIM:240300AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE I, WITH OR WITHOUT REVERSIBLE METAPHYSEAL DYSPLASIA; APS192
HP:0200123HP:0200120Chronic active hepatitis1ALMS1 CL E G H7840428OMIM:203800Alstrom syndrome.404
HP:0200123HP:0200120Chronic active hepatitis1C4B CL E G H7211324OMIM:614379Complement component 4B deficiency.1
HP:0200123HP:0200124Chronic hepatitis due to cryptosporidium infection1CIITA CL E G H42617067ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent118
HP:0200123HP:0200124Chronic hepatitis due to cryptosporidium infection1IL21R CL E G H506156006OMIM:615207IMMUNODEFICIENCY 56; IMD567
HP:0200123HP:0200124Chronic hepatitis due to cryptosporidium infection1RFX5 CL E G H59939986ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent38
HP:0200123HP:0200124Chronic hepatitis due to cryptosporidium infection1RFXANK CL E G H86259987ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent26
HP:0200123HP:0200124Chronic hepatitis due to cryptosporidium infection1RFXAP CL E G H59949988ORPHA:572Immunodeficiency by defective expression of MHC class IIHP:0040282 - Frequent34


Genes (12) :AIRE ALMS1 C4B CD40LG CIITA HBB IL21R PGM1 RFX5 RFXANK RFXAP SKIC2

Diseases (9) :OMIM:240300 OMIM:203800 OMIM:614379 OMIM:308230 ORPHA:572 ORPHA:231226 OMIM:615207 OMIM:614921 OMIM:614602
 

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