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
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Galloway-Mowat syndrome
Summary
Galloway-Mowat syndrome is a designated intractable/rare disease[1]. It draws 33 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 is a type of autosomal recessive disease[6].
- Galloway-Mowat syndrome is a type of syndrome[7].
- Galloway-Mowat syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4468[8].
- Galloway-Mowat syndrome's NCI Thesaurus ID is recorded as C132195[9].
- Galloway-Mowat syndrome's genetic association is recorded as WDR73[10].
- Galloway-Mowat syndrome's genetic association is recorded as OSGEP[11].
- Galloway-Mowat syndrome's genetic association is recorded as TP53RK[12].
- Galloway-Mowat syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2065[13].
- Galloway-Mowat syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080694[14].
- Galloway-Mowat syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080694[15].
- Galloway-Mowat syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Galloway-Mowat syndrome draws 33 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.[17] It is known by 15 alternative names across languages and contexts.[18]