About: MORM syndrome

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MORM syndrome is an autosomal recessive congenital disorder characterized by mental retardation, truncal obesity, , and micropenis". The disorder shares similar characteristics with Bardet–Biedl syndrome and Cohen syndrome, both of which are autosomal recessive genetic disorders. MORM syndrome can be distinguished from the above disorders because symptoms appear at a young age. The disorder is not dependent on sex of the offspring, both male and female offspring are equally likely to inherit the disorder.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalRecessiveDisorders yago:WikicatCongenitalDisorders yago:Abnormality114501726 yago:Abstraction100002137 yago:Anomaly114505821 yago:Attribute100024264 yago:BirthDefect114465048 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Defect114464005 yago:Disease114070360 yago:Disorder114052403 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:Imperfection114462666 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 disease yago:State100024720 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatSyndromes
rdfs:label	MORM-Syndrom (de) MORM syndrome (en) Zespół MORM (pl)
rdfs:comment	Das MORM-Syndrom, Akronym für Mentale Retardierung, rumpfbetonte Obesitas (Stammfettsucht), Retinale Dystrophie und Mikropenis, ist eine sehr seltene angeborene Erkrankung mit den namensgebenden Hauptmerkmalen. Die Erstbeschreibung stammt aus dem Jahre 2006 durch die britischen Ärzte David J. Hampshire, Mohammed Ayub, Kelly Springell und Mitarbeiter. (de) Zespół MORM (ang. MORM syndrome) – rzadki zespół wad wrodzonych, opisany w 2006 roku u czternastu spokrewnionych pacjentów. MORM to akronim od głównych objawów zespołu: opóźnienia umysłowego (mental retardation), otyłości typu centralnego (truncal obesity), dystrofii siatkówki (retinal dystrophy) i nieprawidłowo małego prącia (micropenis). Typowane locus genu odpowiedzialnego za zespół MORM to 9q34. (pl) MORM syndrome is an autosomal recessive congenital disorder characterized by mental retardation, truncal obesity, , and micropenis". The disorder shares similar characteristics with Bardet–Biedl syndrome and Cohen syndrome, both of which are autosomal recessive genetic disorders. MORM syndrome can be distinguished from the above disorders because symptoms appear at a young age. The disorder is not dependent on sex of the offspring, both male and female offspring are equally likely to inherit the disorder. (en)
name	MORM syndrome (en)
foaf:depiction
dcterms:subject	Autosomal recessive disorders Congenital disorders Rare syndromes
Wikipage page ID	18882012 (xsd:integer)
Wikipage revision ID	1091257422 (xsd:integer)
Link from a Wikipage to another Wikipage	Mutation DNA Inheritance Genetic code Genetic disorder Zygosity Autosomal recessive disorders Nucleobase Transition (genetics) Micropenis Bardet–Biedl syndrome Cilium RNA Congenital disorders Rare syndromes Biotechnology Coding region Cohen syndrome Dominance (genetics) Autosome Axoneme Intellectual disability Mental retardation Sequence analysis Exon Congenital abnormality INPP5E Peptide sequence Language comprehension dbr:Retinal_dystrophy dbr:Vision_acuity
sameAs	MORM syndrome MORM syndrome MORM syndrome MORM syndrome MORM syndrome MORM syndrome
dbp:wikiPageUsesTemplate	dbt:Empty_section dbt:Medical_resources dbt:Reflist dbt:Infobox_medical_condition dbt:Medicine
thumbnail	wiki-commons:Special:FilePath/Chromosome_9_Diagram.png?width=300
MeshID	536984.0 (nicaraguanCórdoba)
OMIM	610156 (xsd:integer)
Orphanet	75858 (xsd:integer)
caption	The image shows chromosome 9. The location of the INPP5E gene has been identified in this image and is relevant as it has been associated with MORM syndrome. The gene is located on the Q or long arm of chromosome 9 and is located near 9q34.3. (en)
synonyms	Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome, Mental retardation-truncal obesity-retinal dystrophy-micropenis syndrome (en)
has abstract	Das MORM-Syndrom, Akronym für Mentale Retardierung, rumpfbetonte Obesitas (Stammfettsucht), Retinale Dystrophie und Mikropenis, ist eine sehr seltene angeborene Erkrankung mit den namensgebenden Hauptmerkmalen. Die Erstbeschreibung stammt aus dem Jahre 2006 durch die britischen Ärzte David J. Hampshire, Mohammed Ayub, Kelly Springell und Mitarbeiter. (de) MORM syndrome is an autosomal recessive congenital disorder characterized by mental retardation, truncal obesity, , and micropenis". The disorder shares similar characteristics with Bardet–Biedl syndrome and Cohen syndrome, both of which are autosomal recessive genetic disorders. MORM syndrome can be distinguished from the above disorders because symptoms appear at a young age. The disorder is not dependent on sex of the offspring, both male and female offspring are equally likely to inherit the disorder. The syndrome is caused by a mutation in the INPP5E gene which can be located on chromosome 9 in humans. Further mapping resulted in the identification of a MORM syndrome locus on chromosome 9q34.3 between the genetic markers D9S158 and D9S905. (en) Zespół MORM (ang. MORM syndrome) – rzadki zespół wad wrodzonych, opisany w 2006 roku u czternastu spokrewnionych pacjentów. MORM to akronim od głównych objawów zespołu: opóźnienia umysłowego (mental retardation), otyłości typu centralnego (truncal obesity), dystrofii siatkówki (retinal dystrophy) i nieprawidłowo małego prącia (micropenis). Typowane locus genu odpowiedzialnego za zespół MORM to 9q34. (pl)
MeSH ID	C536984
prov:wasDerivedFrom	wikipedia-en:MORM_syndrome?oldid=1091257422&ns=0
page length (characters) of wiki page	9488 (xsd:nonNegativeInteger)
alias	Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome, Mental retardation-truncal obesity-retinal dystrophy-micropenis syndrome (en)
OMIM id	610156 (xsd:integer)
ORPHA	75858
foaf:isPrimaryTopicOf	wikipedia-en:MORM_syndrome

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