Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
ID

http://purl.bioontology.org/ontology/OMIM/609579
cui

C1865070
Gene Locus

10q26
Gene Symbol

TK14

FGFR2

BEK

BBDS

JWS

CFD1
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

609579
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/C566511 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C566511 Medical Subject Headings LOOM