brown-Vialetto-van Laere syndrome 2
human disease
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brown-Vialetto-van Laere syndrome 2
Summary
brown-Vialetto-van Laere syndrome 2 is a head and neck disease[1].
Key Facts
- brown-Vialetto-van Laere syndrome 2's instance of is recorded as head and neck disease[2].
- brown-Vialetto-van Laere syndrome 2's instance of is recorded as developmental defect during embryogenesis[3].
- brown-Vialetto-van Laere syndrome 2's instance of is recorded as rare disease[4].
- brown-Vialetto-van Laere syndrome 2's instance of is recorded as class of disease[5].
- brown-Vialetto-van Laere syndrome 2 is a type of autosomal recessive disease[6].
- brown-Vialetto-van Laere syndrome 2 is a type of Brown-Vialetto-Van Laere syndrome[7].
- brown-Vialetto-van Laere syndrome 2's NCI Thesaurus ID is recorded as C183529[8].
- brown-Vialetto-van Laere syndrome 2's genetic association is recorded as SLC52A2[9].
- brown-Vialetto-van Laere syndrome 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_97229[10].
- brown-Vialetto-van Laere syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080786[11].
- brown-Vialetto-van Laere syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0080786[12].