autosomal recessive osteopetrosis 7
osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous or compound heterozygous mutation in the TNFRSF11A gene on chromosome 18q21
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autosomal recessive osteopetrosis 7
Summary
autosomal recessive osteopetrosis 7 is a developmental defect during embryogenesis[1].
Key Facts
- autosomal recessive osteopetrosis 7's instance of is recorded as developmental defect during embryogenesis[2].
- autosomal recessive osteopetrosis 7's instance of is recorded as rare disease[3].
- autosomal recessive osteopetrosis 7's instance of is recorded as class of disease[4].
- autosomal recessive osteopetrosis 7 is a type of osteopetrosis[5].
- autosomal recessive osteopetrosis 7 is a type of other immunodeficiency syndrome with predominantly antibody defects[6].
- autosomal recessive osteopetrosis 7 is a type of autosomal recessive disease[7].
- autosomal recessive osteopetrosis 7's health specialty is recorded as medical genetics[8].
- autosomal recessive osteopetrosis 7's genetic association is recorded as TNFRSF11A[9].
- autosomal recessive osteopetrosis 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110946[10].
- autosomal recessive osteopetrosis 7's exact match is recorded as http://identifiers.org/doid/DOID:0110946[11].
- autosomal recessive osteopetrosis 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_178389[12].
- autosomal recessive osteopetrosis 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].