Preferred Name | brachydactyly type A2 | |
Synonyms |
BDA2 Mohr-Wriedt type brachydactyly brachymesophalangy II |
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Definitions |
A brachydactyly characterized by autosomal dominant inheritance of malformations of the middle phalanx of the index finger and anomalies of the second toe that has_material_basis_in heterozygous mutation in the BMPR1B gene on chromosome 4q or in the GDF5 gene on chromosome 20q11 or heterozygous duplication in a regulatory element of BMP2 on chromosome 20p12. |
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ID |
http://purl.obolibrary.org/obo/DOID_0110965 |
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database_cross_reference |
SNOMEDCT_US_2023_03_01:720569006 UMLS_CUI:C1832702 MESH:C537089 GARD:979 MIM:112600 ORDO:93396 |
|
definition |
A brachydactyly characterized by autosomal dominant inheritance of malformations of the middle phalanx of the index finger and anomalies of the second toe that has_material_basis_in heterozygous mutation in the BMPR1B gene on chromosome 4q or in the GDF5 gene on chromosome 20q11 or heterozygous duplication in a regulatory element of BMP2 on chromosome 20p12. |
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has exact synonym |
BDA2 Mohr-Wriedt type brachydactyly brachymesophalangy II |
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has material basis in | ||
has_obo_namespace |
disease_ontology |
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id |
DOID:0110965 |
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in_subset | ||
label |
brachydactyly type A2 |
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notation |
DOID:0110965 |
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prefLabel |
brachydactyly type A2 |
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subClassOf |