Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
Preferred Name

WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 10A

Synonyms

TOOTH AGENESIS, SELECTIVE 4

ID

http://purl.bioontology.org/ontology/OMIM/606268

altLabel

TOOTH AGENESIS, SELECTIVE 4

WNT10A

TOOTH AGENESIS, SELECTIVE, 4, WITH OR WITHOUT ECTODERMAL DYSPLASIA

ODONTOONYCHODERMAL DYSPLASIA

TOOTH AGENESIS, SELECTIVE, 4

SCHOPF-SCHULZ-PASSARGE SYNDROME

cui

C1857069

C1835492

C1422222

C0796093

Gene Locus

2q35

Gene Symbol

WNT10A

STHAG4

OODD

SSPS

Has allelic variant

http://purl.bioontology.org/ontology/OMIM/606268.0001

http://purl.bioontology.org/ontology/OMIM/606268.0005

http://purl.bioontology.org/ontology/OMIM/606268.0006

http://purl.bioontology.org/ontology/OMIM/606268.0007

http://purl.bioontology.org/ontology/OMIM/606268.0002

http://purl.bioontology.org/ontology/OMIM/606268.0003

http://purl.bioontology.org/ontology/OMIM/606268.0009

http://purl.bioontology.org/ontology/OMIM/606268.0008

http://purl.bioontology.org/ontology/OMIM/606268.0004

MIMTYPEMEANING

Gene with known sequence

notation

606268

OMIM Entry Type

1

OMIM MimType Value

star

prefLabel

WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 10A

tui

T028

T047

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http://purl.bioontology.org/ontology/MESH/C537742 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C565607 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C563634 Medical Subject Headings CUI