(Q55345801)

English

Stickler syndrome, type i, nonsyndromic ocular

human disease

Stickler Syndrome, Atypical
Stickler Syndrome, Type I, Predominantly Ocular
Rhegmatogenous Retinal Detachment, Autosomal Dominant
STICKLER SYNDROME, TYPE I, NONSYNDROMIC OCULAR

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subclass of

Stickler syndrome type 1

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

http://www.orpha.net/ORDO/Orphanet_209867

0 references

http://www.orpha.net/ORDO/Orphanet_828

0 references

http://www.orpha.net/ORDO/Orphanet_90653

0 references

Identifiers

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

(Q55345801)

Stickler syndrome, type i, nonsyndromic ocular

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