Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/617238 http://purl.bioontology.org/ontology/OMIM/617238
Preferred Name	MYOPIA 25, AUTOSOMAL DOMINANT
Synonyms	MYP25
Type	http://www.w3.org/2002/07/owl#Class

altLabel	MYP25
prefLabel	MYOPIA 25, AUTOSOMAL DOMINANT
Gene Symbol	MYP25 P4HA2
Scope Statement	Onset of myopia by age 10 years [MISCELLANEOUS] Caused by mutation in the procollagen-proline, 2-oxoglutarate-4-dioxygenase, alpha-subunit, isoform-2 gene (P4HA2, 600608.0001) [MOLECULAR BASIS]
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU002187 http://purl.bioontology.org/ontology/OMIM/MTHU056553
tui	T047
Gene Locus	5q31
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	617238
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T047
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C4310655
OMIM Entry Type	3
OMIM MimType Value	pound

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