All terms in OMIM

Label Id Description
prostate cancer, hereditary, 3 608656
GJC1 608655
AMY1A 104700
neuropathy, hereditary sensory and autonomic, type 5 608654
Hereditary sensory and autonomic neuropathy PS162400
PLEKHA8 608639
asperger syndrome, susceptibility to, 1 608638
Asperger syndrome, susceptibility to PS608638
608637 608637
chromosome 15q11-q13 duplication syndrome 608636
Autism, susceptiblity to PS209850
fetal hemoglobin quantitative trait locus 1 141749
pfeiffer-palm-teller syndrome 261560
ZADH1 608642
deafness, autosomal dominant 28 608641
ZNF461 608640
ciliary dyskinesia, primary, 4 608646
deafness, autosomal dominant 31 608645
ciliary dyskinesia, primary, 3 608644
aromatic l-amino acid decarboxylase deficiency 608643