Online Mendelian Inheritance in Man

Last uploaded: March 22, 2026

Id	http://purl.bioontology.org/ontology/OMIM/102100 http://purl.bioontology.org/ontology/OMIM/102100
Preferred Name	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA
Synonyms	ROSENTHAL-KLOEPFER SYNDROME
Type	http://www.w3.org/2002/07/owl#Class

altLabel	ROSENTHAL-KLOEPFER SYNDROME
prefLabel	ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA
type	http://www.w3.org/2002/07/owl#Class
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU053301 http://purl.bioontology.org/ontology/OMIM/MTHU007719 http://purl.bioontology.org/ontology/OMIM/MTHU053302 http://purl.bioontology.org/ontology/OMIM/MTHU053304 http://purl.bioontology.org/ontology/OMIM/MTHU002089 http://purl.bioontology.org/ontology/OMIM/MTHU002088 http://purl.bioontology.org/ontology/OMIM/MTHU053303 http://purl.bioontology.org/ontology/OMIM/MTHU035887 http://purl.bioontology.org/ontology/OMIM/MTHU006858 See more See less
tui	T019
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	102100
Semantic type UMLS property	http://purl.bioontology.org/ontology/STY/T019
Has inheritance type	http://purl.bioontology.org/ontology/OMIM/MTHU000018
cui	C1321495
OMIM Entry Type	5
OMIM MimType Value	perc

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