Rare Disease Library

Meige disease

Hereditary lymphedema type II · Meige lymphedema

Meigs syndrome

Demons-Meigs syndrome

Myoclonic epilepsy of infancy

Benign myoclonus epilepsy of infancy · Benign myoclonic epilepsy of infancy

Blepharospasm-oromandibular dystonia syndrome

Meige dystonia · Meige syndrome

Ear-patella-short stature syndrome

Meier-Gorlin syndrome

Monomorphic epitheliotropic intestinal T-cell lymphoma

MEITL · Enteropathy-associated T-cell lymphoma type 2

Non-hereditary late-onset primary lymphedema

Meige-like disease

Primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement

FHHNC with severe ocular involvement · Hypercalciuria-bilateral macular coloboma syndrome

Atypical Meigs syndrome

Atypical Demons-Meigs syndrome · Incomplete Meigs syndrome

Bonnemann-Meinecke-Reich syndrome

Encephalopathy-intracerebral calcification-retinal degeneration syndrome

Cleft palate-congenital heart defect-intellectual disability syndrome due to MEIS2 mutation

Familial multiple nevi flammei

Familial multiple port-wine stains

Female infertility due to oocyte meiotic arrest

Male infertility with normal virilization due to meiosis defect

Azoospermia due to maturation arrest · Azoospermia due to meiosis defect

Pseudo-Meigs syndrome

Pseudo-Demons-Meigs syndrome