Human Disease Ontology / 人类疾病本体

Last uploaded: September 7, 2023
Preferred Name

prune belly syndrome

Synonyms

Obrisnksy syndrome

Definitions

A syndrome that is characterized by megacystis with disorganized detrusor muscle, cryptorchidism, and thin abdominal musculature with overlying lax skin and that has_material_basis_in homozygous mutation in the CHRM3 gene on chromosome 1q43.

ID

http://purl.obolibrary.org/obo/DOID_0060889

database_cross_reference

GARD:7479

ORDO:2970

ICD10CM:Q79.4

OMIM:100100

MESH:D011535

definition

A syndrome that is characterized by megacystis with disorganized detrusor muscle, cryptorchidism, and thin abdominal musculature with overlying lax skin and that has_material_basis_in homozygous mutation in the CHRM3 gene on chromosome 1q43.

has exact synonym

Obrisnksy syndrome

abdominal muscle deficiency syndrome

Eagle-Barret syndrome

has material basis in

http://purl.obolibrary.org/obo/GENO_0000148

has_obo_namespace

disease_ontology

id

DOID:0060889

in_subset

http://purl.obolibrary.org/obo/doid#DO_rare_slim

label

prune belly syndrome

notation

DOID:0060889

prefLabel

prune belly syndrome

subClassOf

http://purl.obolibrary.org/obo/DOID_225

http://purl.obolibrary.org/obo/DOID_0050737

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http://purl.bmicc.cn/ontology/ICD11CN/LD2F.10 《国际疾病分类》第11版中文版 / International Classification of Diseases, 11th Edition, China LOOM
http://purl.bioontology.org/ontology/ICD10/Q79.4 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85033 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://www.orpha.net/ORDO/Orphanet_2970 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0007032 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.obolibrary.org/obo/MONDO_0007032 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.bioontology.org/ontology/OMIM/100100 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU070711 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM
http://purl.bioontology.org/ontology/MESH/D011535 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q79.4 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 LOOM