focal dermal hypoplasia Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2120)
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22 genes co-occuring with the disease focal dermal hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
PORCN porcupine homolog (Drosophila) 2.90967
ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide 2.30396
IKBKG inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma 1.9727
MSL3 male-specific lethal 3 homolog (Drosophila) 1.73595
MSL2 male-specific lethal 2 homolog (Drosophila) 1.50535
WLS wntless Wnt ligand secretion mediator 1.24341
GOLPH3 golgi phosphoprotein 3 (coat-protein) 1.22128
WNT3A wingless-type MMTV integration site family, member 3A 1.0816
HCCS holocytochrome c synthase 0.9839
PCDH19 protocadherin 19 0.980531
OFD1 oral-facial-digital syndrome 1 0.891718
ORM1 orosomucoid 1 0.877786
HOXB4 homeobox B4 0.862637
AMER1 APC membrane recruitment protein 1 0.848307
MBTPS2 membrane-bound transcription factor peptidase, site 2 0.847488
COL5A1 collagen, type V, alpha 1 0.799513
AK1 adenylate kinase 1 0.761862
ATP7A ATPase, Cu++ transporting, alpha polypeptide 0.643404
STS steroid sulfatase (microsomal), isozyme S 0.457487
PTER phosphotriesterase related 0.442418
COL1A2 collagen, type I, alpha 2 0.233878
GJA1 gap junction protein, alpha 1, 43kDa 0.215653