About: Saal Greenstein syndrome

An Entity of Type: disease, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

Saal Greenstein syndrome is a very rare autosomal recessive genetic disorder characterized by stunted growth, short limbs, microcephaly, and an anomalous cleavage of the anterior chamber of the eye. The disorder is similar to Robinow syndrome except for anterior chamber anomalies and, in one case, hydrocephalus.

Property	Value
dbo:abstract	Saal Greenstein syndrome is a very rare autosomal recessive genetic disorder characterized by stunted growth, short limbs, microcephaly, and an anomalous cleavage of the anterior chamber of the eye. The disorder is similar to Robinow syndrome except for anterior chamber anomalies and, in one case, hydrocephalus. (en)
dbo:icd10	Q87.1
dbo:orpha	3105
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dbo:wikiPageWikiLink	dbr:Anterior_chamber_of_eyeball dbr:Hydrocephalus dbr:Robinow_syndrome dbc:Genetic_diseases_and_disorders dbc:Rare_diseases dbc:Syndromes dbr:Microcephaly dbr:Anterior_chamber
dbp:caption	Autosomal recessive is the manner of inheritance of this condition (en)
dbp:icd	Q87.1 (en)
dbp:imageSize	140 (xsd:integer)
dbp:name	Saal Greenstein syndrome (en)
dbp:orphanet	3105 (xsd:integer)
dbp:synonyms	Robinow-like syndrome (en)
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rdfs:comment	Saal Greenstein syndrome is a very rare autosomal recessive genetic disorder characterized by stunted growth, short limbs, microcephaly, and an anomalous cleavage of the anterior chamber of the eye. The disorder is similar to Robinow syndrome except for anterior chamber anomalies and, in one case, hydrocephalus. (en)
rdfs:label	Saal Greenstein syndrome (en)
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foaf:name	Saal Greenstein syndrome (en)
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