About: Usher syndrome type 1

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An Entity of Type : about:cgab#this, within Data Space : semmed.demo.openlinksw.com associated with source document(s)

Attributes	Values
type	cgab
label	Usher syndrome type 1 usher syndrome type 1
http://semmed.demo...com/terms#part_of	C0030705
terms:part_of	C0030705 Family Child Persons
terms:causes	Blind Vision Deafness
terms:manifestation_of	Mutation
schema:identifier	C0339533 c0339533
PART_OF	C0030705 Family Child Persons
is http://semmed.demo...m/terms#diagnoses of	mutation analysis
is terms:causes of	myosin VIIa\|MYO7A
is terms:location_of of	Family Child
is terms:coexists_with of	Functional disorder Aplasia, NOS Sensorineural Hearing Loss Cataract Congenital deafness HEARING LOSS CONGENITAL
is terms:diagnoses of	Tomography, Optical Coherence mutation analysis Molecular Diagnosis
is LOCATION_OF of	Family Child
is COEXISTS_WITH of	Functional disorder HEARING LOSS CONGENITAL
is DIAGNOSES of	mutation analysis

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