Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	Retinal dysplasia
ID	http://purl.bioontology.org/ontology/OMIM/MTHU020469
cui	C0035313
Manifestation of	http://purl.bioontology.org/ontology/OMIM/310600 http://purl.bioontology.org/ontology/OMIM/615665 http://purl.bioontology.org/ontology/OMIM/615041 http://purl.bioontology.org/ontology/OMIM/615287 http://purl.bioontology.org/ontology/OMIM/614830 http://purl.bioontology.org/ontology/OMIM/613154 http://purl.bioontology.org/ontology/OMIM/614643
notation	MTHU020469
prefLabel	Retinal dysplasia
tui	T019
subClassOf	http://purl.bioontology.org/ontology/OMIM/MTHU000020

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/HP_0007973	Human Phenotype Ontology	LOOM
http://purl.bioontology.org/ontology/MESH/D015792	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D015792	Medical Subject Headings	LOOM