Galloway-Mowat syndrome
autosomal recessive disease characterized by is a rare autosomal recessive disease, characterized by microcephaly with brain anomalies including CA in some cases, intellectual disability, and early-infantile-onset nephrotic syndrome
Press Enter · cited answer in seconds
0 sources
Galloway-Mowat syndrome
Summary
Galloway-Mowat syndrome is a designated intractable/rare disease[1]. It draws 6 Wikipedia views per month (designated_intractable_rare_disease category, ranking #166 of 201).[2]
Key Facts
- Galloway-Mowat syndrome's instance of is recorded as designated intractable/rare disease[3].
- Galloway-Mowat syndrome's instance of is recorded as rare disease[4].
- Galloway-Mowat syndrome's instance of is recorded as class of disease[5].
- Galloway-Mowat syndrome's subclass of is recorded as autosomal recessive disease[6].
- Galloway-Mowat syndrome's subclass of is recorded as syndrome[7].
- Galloway-Mowat syndrome's MeSH descriptor ID is recorded as C537548[8].
- Galloway-Mowat syndrome's OMIM ID is recorded as 251300[9].
- Galloway-Mowat syndrome's DiseasesDB is recorded as 31334[10].
- Galloway-Mowat syndrome's Freebase ID is recorded as /m/0bvkdg[11].
- Galloway-Mowat syndrome's KEGG ID is recorded as H01722[12].
- Galloway-Mowat syndrome's Disease Ontology ID is recorded as DOID:0080694[13].
- Galloway-Mowat syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4468[14].
- Galloway-Mowat syndrome's Orphanet ID is recorded as 2065[15].
- Galloway-Mowat syndrome's NCI Thesaurus ID is recorded as C132195[16].
- Galloway-Mowat syndrome's genetic association is recorded as WDR73[17].
- Galloway-Mowat syndrome's genetic association is recorded as OSGEP[18].
- Galloway-Mowat syndrome's genetic association is recorded as TP53RK[19].
- Galloway-Mowat syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2065[20].
- Galloway-Mowat syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080694[21].
- Galloway-Mowat syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080694[22].
- Galloway-Mowat syndrome's UMLS CUI is recorded as C0795949[23].
- Galloway-Mowat syndrome's ICD-10-CM is recorded as Q04.3[24].
- Galloway-Mowat syndrome's GARD rare disease ID is recorded as 65[25].
- Galloway-Mowat syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[26].
- Galloway-Mowat syndrome's Mondo ID is recorded as MONDO_0009627[27].
Why It Matters
Galloway-Mowat syndrome draws 6 Wikipedia views per month (designated_intractable_rare_disease category, ranking #166 of 201).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] It is known by 15 alternative names across languages and contexts.[29]