Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/OMIM/620910
http://purl.bioontology.org/ontology/OMIM/620910
Preferred Name

OTOFACIAL NEURODEVELOPMENTAL SYNDROME
Synonyms
OFNS
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
OFNS
prefLabel
OTOFACIAL NEURODEVELOPMENTAL SYNDROME
Gene Symbol
OFNS
ZSCAN10
ZFP206
Scope Statement
Caused by mutation in the zinc finger- and SCAN domain-containing protein 10 gene (ZSCAN10, 618365.0001) [MOLECULAR BASIS]
Onset in infancy [MISCELLANEOUS]
type
Has manifestation
http://purl.bioontology.org/ontology/OMIM/MTHU000231
http://purl.bioontology.org/ontology/OMIM/MTHU079124
http://purl.bioontology.org/ontology/OMIM/MTHU000691
http://purl.bioontology.org/ontology/OMIM/MTHU012400
http://purl.bioontology.org/ontology/OMIM/MTHU008495
http://purl.bioontology.org/ontology/OMIM/MTHU035437
http://purl.bioontology.org/ontology/OMIM/MTHU038499
http://purl.bioontology.org/ontology/OMIM/MTHU036353
http://purl.bioontology.org/ontology/OMIM/MTHU079125
http://purl.bioontology.org/ontology/OMIM/MTHU005818
http://purl.bioontology.org/ontology/OMIM/MTHU079122
http://purl.bioontology.org/ontology/OMIM/MTHU012538
http://purl.bioontology.org/ontology/OMIM/MTHU002513
http://purl.bioontology.org/ontology/OMIM/MTHU063892
http://purl.bioontology.org/ontology/OMIM/MTHU000574
http://purl.bioontology.org/ontology/OMIM/MTHU003212
http://purl.bioontology.org/ontology/OMIM/MTHU079123
http://purl.bioontology.org/ontology/OMIM/MTHU032883
http://purl.bioontology.org/ontology/OMIM/MTHU070919
http://purl.bioontology.org/ontology/OMIM/MTHU000064
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tui
T047
Gene Locus
16p13.3
MIMTYPEMEANING
Phenotype description, molecular basis known.
notation
620910
Semantic type UMLS property
Has inheritance type
cui
C5935642
OMIM Entry Type
3
OMIM MimType Value
pound
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