Laurin-Sandrow syndrome
ORPHA:2378Legius syndrome
ORPHA:137605Leigh syndrome
ORPHA:506Lelis syndrome
ORPHA:140936Lethal Larsen-like syndrome
ORPHA:2371Leukocyte adhesion deficiency type II
ORPHA:99843Leukoencephalopathy with calcifications and cysts
ORPHA:542310Li-Fraumeni syndrome
ORPHA:524Liddle syndrome
ORPHA:526LIG4 syndrome
ORPHA:99812Limb body wall complex
ORPHA:2369Linear nevus sebaceus syndrome
ORPHA:2612LUMBAR syndrome
ORPHA:83628Lynch syndrome
ORPHA:144Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299Mohr-Tranebjaerg syndrome
ORPHA:52368Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Mosaic Legius syndrome
ORPHA:634511Muenke syndrome
ORPHA:53271Multiple endocrine neoplasia type 2A
ORPHA:247698Multiple synostoses syndrome
ORPHA:3237Muscle-eye-brain disease
ORPHA:588Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
ORPHA:86841Myhre syndrome
ORPHA:2588N syndrome
ORPHA:2608Naegeli-Franceschetti-Jadassohn syndrome
ORPHA:69087NAME syndrome
ORPHA:623NARP syndrome
ORPHA:644Nelson syndrome
ORPHA:199244Neu-Laxova syndrome
ORPHA:2671Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome with multiple lentigines
ORPHA:500Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972NPHP3-related Meckel-like syndrome
ORPHA:3032Oculocerebrorenal syndrome of Lowe
ORPHA:534Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Otofaciocervical syndrome
ORPHA:2792Pai syndrome
ORPHA:1993