Annotation Detail

Information
Associated Genes
STAMBP
Associated Variants
STAMBP MUTATION
STAMBP MUTATION
Associated Disease
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
Source Database
DisGeNET
Description
Herein, we describe an Arab family of two siblings with classic features of MIC-CAP syndrome that harbor a novel predicted splice mutation in STAMBP, which additionally display previously unreported findings of congenital hypothyroidism and alopecia areata.
Pubmed
25692795
Section of the abstract supporting the evidence
ALL_TEXT_3/3
Number of the section of the abstract supporting the evidence
3
Number of the sentence supporting the evidence
4
Original source reporting the Gene Disease association
BeFree
DisGENET score for the Gene Disease association
0.000271441872080303
Drugs