Preferred Name

Prune Belly Syndrome

ID

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C85033

ALT_DEFINITION

A congenital syndrome, occurring almost exclusively in males, characterized by partial or complete absence of the abdominal wall muscles, enlarged bladder, dilated ureters, hydronephrosis, and undescended testes, with or without renal insufficiency.

code

C85033

Concept_In_Subset

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C123272

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C192842

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C165258

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C90259

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C99147

Contributing_Source

NICHD

Cellosaurus

DEFINITION

A rare congenital syndrome occurring almost exclusively in males. It is characterized by partial or complete lack of the abdominal wall muscles, enlarged bladder, dilated ureters, hydronephrosis, and undescended testes.

FULL_SYN

Eagle-Barrett Syndrome

Triad Syndrome

Syndrome of Agenesis of Abdominal Muscles

Prune Belly Syndrome

label

Prune Belly Syndrome

Preferred_Name

Prune Belly Syndrome

prefixIRI

Thesaurus:C85033

prefLabel

Prune Belly Syndrome

Semantic_Type

Disease or Syndrome

UMLS_CUI

C4225641

subClassOf

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C53543

http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C28193

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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://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.obolibrary.org/obo/DOID_0060889 Human Disease Ontology / 人类疾病本体 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