Preferred Name

nebulin

ID

http://www.orpha.net/ORDO/Orphanet_123749

alternative_term

nemaline myopathy type 2

NEB177D

hasDbXref

HGNC:7720

OMIM:161650

Ensembl:ENSG00000183091

Genatlas:NEB

Reactome:P20929

SwissProt:P20929

label

nebulin

prefixIRI

ORDO:Orphanet_123749

prefLabel

nebulin

symbol

NEB

subClassOf

http://www.orpha.net/ORDO/Orphanet_410298

Delete Subject Author Type Created
No notes to display
Create New Mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/C035620 Medical Subject Headings / 医学主题词表 LOOM
http://purl.obolibrary.org/obo/PR_000011107 Protein Ontology / 蛋白质本体 LOOM
http://purl.obolibrary.org/obo/PR_000011107 中国人类表型本体 / Human Phenotype Ontology China LOOM
http://purl.org/sig/ont/fma/fma62383 Foundational Model of Anatomy / 解剖学基础模型本体 LOOM
http://purl.bioontology.org/ontology/OMIM/161650 Online Mendelian Inheritance in Man / 在线人类孟德尔遗传数据库 LOOM