Laron syndrome
ORPHA:633Laron syndrome with immunodeficiency
ORPHA:220465Larsen syndrome
ORPHA:503Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lateral meningocele syndrome
ORPHA:2789Laurin-Sandrow syndrome
ORPHA:2378Legius syndrome
ORPHA:137605Leigh syndrome
ORPHA:506Lelis syndrome
ORPHA:140936Lethal ataxia with deafness and optic atrophy
ORPHA:1187Leukoencephalopathy with calcifications and cysts
ORPHA:542310Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816Li-Fraumeni syndrome
ORPHA:524Liddle syndrome
ORPHA:526LIG4 syndrome
ORPHA:99812Limb body wall complex
ORPHA:2369LUMBAR syndrome
ORPHA:83628Lynch syndrome
ORPHA:144Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Metaphyseal chondrodysplasia, Rosenberg type
ORPHA:1837Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299MOMO syndrome
ORPHA:2563Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112MRCS syndrome
ORPHA:263347Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Muscle-eye-brain disease
ORPHA:588Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841N syndrome
ORPHA:2608Naegeli-Franceschetti-Jadassohn syndrome
ORPHA:69087NAME syndrome
ORPHA:623NARP syndrome
ORPHA:644Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome with multiple lentigines
ORPHA:500Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Null syndrome
ORPHA:280234Oculocerebrorenal syndrome of Lowe
ORPHA:534