Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024

Preferred Name	PROSOPAGNOSIA, HEREDITARY
Synonyms	PROSOPAGNOSIA, CONGENITAL
ID	http://purl.bioontology.org/ontology/OMIM/610382
altLabel	PROSOPAGNOSIA, CONGENITAL FACE BLINDNESS PROSOPAGNOSIA, DEVELOPMENTAL
cui	C0234512 C2931455 C0751842
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU039049
MIMTYPEMEANING	Mendelian phenotype or locus, molecular basis unknown.
notation	610382
OMIM Entry Type	5
OMIM MimType Value	perc
prefLabel	PROSOPAGNOSIA, HEREDITARY
tui	T047 T048

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MDRGER/10073980	MDRGER	CUI
http://purl.bioontology.org/ontology/MESH/C537242	MESH	CUI
http://purl.bioontology.org/ontology/MSHFRE/D020238	MSHFRE	CUI
http://purl.bioontology.org/ontology/NDFRT/N0000004068	NDFRT	CUI
http://purl.bioontology.org/ontology/MSHFRE/D020238	MSHFRE	CUI
http://purl.bioontology.org/ontology/RCD/Xa3EI	RCD	CUI
http://purl.bioontology.org/ontology/MESH/D020238	MESH	CUI
http://purl.bioontology.org/ontology/MEDDRA/10073980	MEDDRA	CUI
http://purl.bioontology.org/ontology/MDRFRE/10073980	MDRFRE	CUI
http://purl.bioontology.org/ontology/SNMI/F-A6540	SNMI	CUI
http://purl.bioontology.org/ontology/SCTSPA/18358003	SCTSPA	CUI
http://purl.bioontology.org/ontology/ICD10CM/R48.3	ICD10CM	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/18358003	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/MESH/D020238	MESH	CUI
http://purl.obolibrary.org/obo/MONDO_0012484	MONDO	LOOM
http://purl.bioontology.org/ontology/MESH/C537242	MESH	LOOM
http://purl.obolibrary.org/obo/MONDO_0012484	DOVES	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C537242	RH-MESH	LOOM