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Galloway-Mowat syndrome - Ontology Report - Rat Genome Database

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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:Galloway-Mowat syndrome
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Accession:EFO:MONDO:0009627 term browser browse the term
Definition:Galloway syndrome is characterized by the association of nephrotic syndrome and central nervous system anomalies.
Synonyms:exact_synonym: DOID:0080694;   Galloway syndrome;   NCIT:C132195;   Orphanet:2065;   http://identifiers.org/medgen/167086;   http://identifiers.org/mesh/C537548;   http://identifiers.org/snomedct/721297008;   http://linkedlifedata.com/resource/umls/id/C0795949;   https://omim.org/phenotypicSeries/PS251300;   microcephaly-hiatus hernia-nephrotic syndrome;   spinocerebellar ataxia, autosomal recessive 5
 related_synonym: GAMOS;   cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities;   cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities;   hiatal hernia-microcephaly-nephrosis, Galloway type;   microcephaly nephrosis syndrome;   microcephaly, hiatal hernia, and nephrotic syndrome;   nephrosis neuronal dysmigration syndrome;   spinocerebellar ataxia, autosomal recessive 5, formerly
 alt_id: MONDO:0009627
 xref: DOID:0080694;   GARD:65;   MEDGEN:167086;   MESH:C537548;   MIM:PS251300;   NANDO:1200713;   NANDO:2200120;   NANDO:2201385;   NCI:C132195;   NORD:1171;   ORDO:2065;   SCTID:721297008;   UMLS:C0795949

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            Galloway-Mowat syndrome 0
              Galloway-Mowat syndrome 10 0
              Galloway-Mowat syndrome 2, X-linked 0
              Galloway-Mowat syndrome 9 0
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              autosomal recessive disease 0
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                  Galloway-Mowat syndrome 10 0
                  Galloway-Mowat syndrome 2, X-linked 0
                  Galloway-Mowat syndrome 9 0
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