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| Term | thrombocytopenia-absent radius syndrome | ID (Ontology) | DOID:14699 (Human Disease) |
| Definition | A chromosomal deletion syndrome that is characterized by absence of the radius bone and platelet deficiency and bilateral absence of the radii with the presence of both thumbs and generally transient thrombocytopenia (less than 50 platelets/nL) and that has_material_basis_in compound heterozygosity for a rare null mutation involving the RBM8A gene on chromosome 1q12 on 1 allele and 1 of 2 low-frequency noncoding single-nucleotide polymorphisms in RBM8A on the other. | ||
| Also Known As | "Radial aplasia-thrombocytopenia syndrome" ; "Thrombocytopenia with absent radii (TAR) syndrome" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease____ chromosomal disease | |__chromosomal deletion syndrome__| disease | |__syndrome_______________________| thrombocytopenia-absent radius syndrome 1 rec. |
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autosomal recessive disease chromosomal deletion syndrome syndrome |
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ICD10CM:Q87.2 MESH:C536940 MIM:274000 NCI:C99038 ORDO:3320 SNOMEDCT_US_2023_03_01:85589009 UMLS_CUI:C0175703 |
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