abnormalities, multiple (3)
germ-line mutation (3)
hand deformities, congenital (3)
melanoma (3)
dna-binding proteins (2)
ehlers-danlos syndrome (2)
genetic predisposition to disease (2)
hemochromatosis (2)
inheritance patterns (2)
intellectual disability (2)
joint instability (2)
micrognathism (2)
transcription factors (2)
ainhum (1)
alopecia (1)
asbestos (1)
autism spectrum disorder (1)
breast neoplasms (1)
cation transport proteins (1)
cell cycle proteins (1)
choroideremia (1)
chromosomes, human, x (1)
congenital hyperinsulinism (1)
craniofacial abnormalities (1)
cyclin-dependent kinase inhibitor p16 (1)
cytoskeletal proteins (1)
dyslipidemias (1)
environmental exposure (1)
epigenesis, genetic (1)
face (1)
fibromatosis, gingival (1)
fingers (1)
foot deformities, congenital (1)
genes, recessive (1)
hair diseases (1)
hypotrichosis (1)
keratoderma, palmoplantar (1)
langer-giedion syndrome (1)
mesothelioma (1)
mutation (1)
neck (1)
neoplasms, multiple primary (1)
neoplastic syndromes, hereditary (1)
nose (1)
nuclear pore complex proteins (1)
pancreatic neoplasms (1)
phenotype (1)
protein serine-threonine kinases (1)
receptor, epha5 (1)
receptors, transferrin (1)