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Preferred Name

NEBULIN
Synonyms

ARTHROGRYPOSIS MULTIPLEX CONGENITA 6
ID

http://purl.bioontology.org/ontology/OMIM/161650
altLabel

ARTHROGRYPOSIS MULTIPLEX CONGENITA 6

NEMALINE MYOPATHY 2

NEB
cui

C1417656

C5543431

C1850569
Gene Locus

2q22
Gene Symbol

AMC6

NEM2

NEB
Has allelic variant

http://purl.bioontology.org/ontology/OMIM/161650.0001

http://purl.bioontology.org/ontology/OMIM/161650.0003

http://purl.bioontology.org/ontology/OMIM/161650.0002

http://purl.bioontology.org/ontology/OMIM/161650.0014

http://purl.bioontology.org/ontology/OMIM/161650.0016

http://purl.bioontology.org/ontology/OMIM/161650.0010

http://purl.bioontology.org/ontology/OMIM/161650.0008

http://purl.bioontology.org/ontology/OMIM/161650.0015

http://purl.bioontology.org/ontology/OMIM/161650.0009

http://purl.bioontology.org/ontology/OMIM/161650.0012

http://purl.bioontology.org/ontology/OMIM/161650.0011

http://purl.bioontology.org/ontology/OMIM/161650.0013

http://purl.bioontology.org/ontology/OMIM/161650.0005

http://purl.bioontology.org/ontology/OMIM/161650.0006

http://purl.bioontology.org/ontology/OMIM/161650.0004

http://purl.bioontology.org/ontology/OMIM/161650.0007
MIMTYPEMEANING

Gene with known sequence
notation

161650
OMIM Entry Type

1
OMIM MimType Value

star
prefLabel

NEBULIN
tui

T028

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/C538349 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/C035620 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/LNC/LP36764-6 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 CUI
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://www.orpha.net/ORDO/Orphanet_123749 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM
http://purl.org/sig/ont/fma/fma62383 Foundational Model of Anatomy / 解剖学基础模型本体 LOOM