Monomelic amyotrophy

Disease Term Disease ID Gene Symbol Classification References Source
AMYOTROPHY, HEREDITARY NEURALGIC
162100C1834304
SEPTIN9 Unknown — Disgenet HPO
AMYOTROPHY, MONOMELIC
C1865384
ARPP21 Unknown — Disgenet
CEP126 Unknown — Disgenet
CPLANE1 Unknown — Disgenet
RYR3 Unknown — Disgenet
SLIT1 Unknown — Disgenet