Fowler syndrome

Summary

Fowler syndrome is a hereditary disorder^[1]. It is known by 13 alternative names across languages and contexts.^[2]

Key Facts

• Fowler syndrome's instance of is recorded as hereditary disorder^[3].
• Fowler syndrome's instance of is recorded as rare disease^[4].
• Fowler syndrome's instance of is recorded as class of disease^[5].
• Fowler syndrome is a type of vascular disease^[6].
• Fowler syndrome is a type of autosomal recessive disease^[7].
• Fowler syndrome is a type of syndrome^[8].
• Fowler syndrome's genetic association is recorded as FLVCR2^[9].
• Fowler syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_221126^[10].
• Fowler syndrome's exact match is recorded as http://purl.obolibrary.org/obo/MONDO_0009168^[11].
• Fowler syndrome's exact match is recorded as http://identifiers.org/mesh/C565593^[12].
• Fowler syndrome's exact match is recorded as http://identifiers.org/omim/225790^[13].
• Fowler syndrome's exact match is recorded as http://identifiers.org/meddra/10071718^[14].
• Fowler syndrome's exact match is recorded as http://linkedlifedata.com/resource/umls/id/C3203738^[15].
• Fowler syndrome's exact match is recorded as http://identifiers.org/snomedct/700242002^[16].
• Fowler syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111666^[17].
• Fowler syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111666^[18].

Why It Matters

Fowler syndrome is known by 13 alternative names across languages and contexts.^[2]