sclerosteosis 2
sclerosteosis that has material basis in heterozygous or homozygous mutation in the LRP4 gene on chromosome 11p11
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sclerosteosis 2
Summary
sclerosteosis 2 is a rare disease[1]. It is known by 4 alternative names across languages and contexts.[2]
Key Facts
- sclerosteosis 2's instance of is recorded as rare disease[3].
- sclerosteosis 2's instance of is recorded as class of disease[4].
- sclerosteosis 2 is a type of sclerosteosis[5].
- sclerosteosis 2 is a type of genetic disease[6].
- sclerosteosis 2 is a type of autosomal dominant disease[7].
- sclerosteosis 2 is a type of autosomal recessive disease[8].
- sclerosteosis 2's genetic association is recorded as LRP4[9].
- sclerosteosis 2's exact match is recorded as http://identifiers.org/doid/DOID:0060757[10].
- sclerosteosis 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060757[11].
- sclerosteosis 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
sclerosteosis 2 is known by 4 alternative names across languages and contexts.[2]