Preferred Name

OBESITY

Synonyms

LEANNESS

ID

http://purl.bioontology.org/ontology/OMIM/601665

altLabel

LEANNESS

cui

C0039870

C0028754

Gene Locus

3p26-p25

Gene Symbol

GHRL

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU000250

http://purl.bioontology.org/ontology/OMIM/MTHU049558

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

601665

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

OBESITY

Scope Statement

Caused by mutation in the nuclear receptor subfamily 0, group B, member 2 gene (NR0B2, 604630.0001) [MOLECULAR BASIS]

Caused by mutation in the gamma peroxisome proliferator activated receptor gene (PPARG, 601487.0001) [MOLECULAR BASIS]

Susceptibility conferred by mutation in the cocaine- and amphetamine-regulated transcript prepropeptide (CARTPT, 602606.0001) [MOLECULAR BASIS]

Susceptibility conferred by mutation in the beta-3-adrenergic receptor gene (ADRB3, 109691.0001) [MOLECULAR BASIS]

Susceptibility conferred by mutation in the uncoupling protein-1 gene (UCP1, 113730.0001) [MOLECULAR BASIS]

Susceptibility conferred by mutation in the ghrelin gene (GHRL, 605353.0001) [MOLECULAR BASIS]

Susceptibility conferred by mutation in the homolog of the mouse agouti gene (AGRP, 602311.0001) [MOLECULAR BASIS]

Susceptibility conferred by mutation in the ectonucleotide pyrophosphatase/phosphodiesterase 1 gene (ENPP1, 173335.0001) [MOLECULAR BASIS]

See also leptin deficiency (614962) and summary information in BMIQ1 (606641) [MISCELLANEOUS]

Susceptibility conferred by mutation in the beta-2-adrenergic receptor gene (ADRB2, 109690.0002) [MOLECULAR BASIS]

Caused by mutation in the melanocortin-4 receptor gene (MC4R, 155541.0001) [MOLECULAR BASIS]

Susceptibility conferred by mutation in the proopiomelanocortin gene (POMC, 176830.0001) [MOLECULAR BASIS]

Variable phenotypic severity [MISCELLANEOUS]

Susceptibility conferred by mutation in the uncoupling protein-2 gene (UCP2, 601693.0001) [MOLECULAR BASIS]

Caused by mutation in the uncoupling protein-3 gene (UCP3, 602044.0001) [MOLECULAR BASIS]

tui

T033

T047

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http://purl.bioontology.org/ontology/MESH/D013851 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/ICD10CM/E66.9 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/LNC/LA6301-1 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.bioontology.org/ontology/LNC/LA6301-1 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bmicc.cn/ontology/ICD11CN/5B81 《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/MESH/D009765 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D009765 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/LNC/LA20940-5 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
http://purl.obolibrary.org/obo/DOID_9970 BioAssay Ontology / 生物活性分析本体 LOOM
http://purl.obolibrary.org/obo/DOID_9970 Human Disease Ontology / 人类疾病本体 LOOM
http://purl.bmicc.cn/ontology/ICD10CN/E66 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bmicc.cn/ontology/ICD10CN/E66.9 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C3283 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0028754 MedlinePlus Health Topics / MedlinePlus网站健康主题 CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0028754 MedlinePlus Health Topics / MedlinePlus网站健康主题 LOOM
http://www.ebi.ac.uk/efo/EFO_0001073 Experimental Factor Ontology / 实验性因素本体 LOOM
http://purl.obolibrary.org/obo/HP_0001513 中国人类表型本体 / Human Phenotype Ontology China LOOM
http://purl.obolibrary.org/obo/HP_0001513 Coronavirus Infectious Disease Ontology / 冠状病毒感染性疾病本体 LOOM
http://purl.obolibrary.org/obo/HP_0001513 Human Phenotype Ontology / 人类表型本体 LOOM
http://purl.obolibrary.org/obo/HP_0001513 GenEpiO / 基因组流行病学本体 LOOM
http://OntoTCM.org.cn/ontologies/TCM_DO_0002168 中医疾病本体 LOOM
http://purl.bioontology.org/ontology/ICD10/E66 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI
http://purl.bioontology.org/ontology/ICD10/E66 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 LOOM
http://purl.bioontology.org/ontology/ICD10/E66.9 International Classification of Diseases, Version 10 / 《国际疾病分类》第10版 CUI