albright's hereditary osteodystrophy Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An osteochondrodysplasia that has_material_basis_in lack of responsiveness to parathyroid hormone which results_in shortening and widening of long bones of the located_in hand or located_in foot along with short stature, obesity, and rounded face. (Human Disease Ontology, DOID_0080053)
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28 genes co-occuring with the disease albright's hereditary osteodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GNAS GNAS complex locus 2.95262
STX16 syntaxin 16 2.01522
PTH parathyroid hormone 1.87883
GNA15 guanine nucleotide binding protein (G protein), alpha 15 (Gq class) 1.57512
GNA11 guanine nucleotide binding protein (G protein), alpha 11 (Gq class) 1.54142
ADCY2 adenylate cyclase 2 (brain) 1.33196
FARP2 FERM, RhoGEF and pleckstrin domain protein 2 1.15283
ETV2 ets variant 2 1.10594
GHRH growth hormone releasing hormone 1.06648
D2HGDH D-2-hydroxyglutarate dehydrogenase 0.932898
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha 0.869187
PRLH prolactin releasing hormone 0.774523
HDAC4 histone deacetylase 4 0.677903
KIF1A kinesin family member 1A 0.626888
TWIST2 twist family bHLH transcription factor 2 0.583552
GRB10 growth factor receptor-bound protein 10 0.529608
BMP4 bone morphogenetic protein 4 0.397098
PDE4D phosphodiesterase 4D, cAMP-specific 0.309566
TSHR thyroid stimulating hormone receptor 0.305587
CAPN10 calpain 10 0.288668
PDCD1 programmed cell death 1 0.285802
NR5A1 nuclear receptor subfamily 5, group A, member 1 0.280439
ADO 2-aminoethanethiol (cysteamine) dioxygenase 0.245046
MC4R melanocortin 4 receptor 0.230409
TEF thyrotrophic embryonic factor 0.209918
NOG noggin 0.172291
TRH thyrotropin-releasing hormone 0.160948
NR0B1 nuclear receptor subfamily 0, group B, member 1 0.158434