Preferred Name

OFD1 CENTRIOLE AND CENTRIOLAR SATELLITE PROTEIN

Synonyms

OROFACIODIGITAL SYNDROME I

ID

http://purl.bioontology.org/ontology/OMIM/300170

altLabel

OROFACIODIGITAL SYNDROME I

RETINITIS PIGMENTOSA 23

CHROMOSOME X OPEN READING FRAME 5

OFD1

SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2

CXORF5

JOUBERT SYNDROME 10

OFD1 GENE

cui

C1413833

C1846175

C1510460

C2749019

C1419610

Gene Locus

Xp22.3-p22.2

Gene Symbol

JBTS10

SGBS2

RP23

OFD1

CXorf5

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/300170.0009

http://purl.bioontology.org/ontology/OMIM/300170.0010

http://purl.bioontology.org/ontology/OMIM/300170.0011

http://purl.bioontology.org/ontology/OMIM/300170.0004

http://purl.bioontology.org/ontology/OMIM/300170.0006

http://purl.bioontology.org/ontology/OMIM/300170.0005

http://purl.bioontology.org/ontology/OMIM/300170.0001

http://purl.bioontology.org/ontology/OMIM/300170.0002

http://purl.bioontology.org/ontology/OMIM/300170.0003

http://purl.bioontology.org/ontology/OMIM/300170.0007

http://purl.bioontology.org/ontology/OMIM/300170.0008

MIMTYPEMEANING

Gene with known sequence

notation

300170

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

OFD1 CENTRIOLE AND CENTRIOLAR SATELLITE PROTEIN

tui

T028

T047

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/D009958 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/C567582 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/C564567 Medical Subject Headings / 医学主题词表 CUI
http://www.orpha.net/ORDO/Orphanet_123982 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM