Kenny-Caffey syndrome
ORPHA:2333Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
ORPHA:281201Keutel syndrome
ORPHA:85202KID syndrome
ORPHA:477Kindler epidermolysis bullosa
ORPHA:2908Kjellin syndrome
ORPHA:100996Kostmann syndrome
ORPHA:99749Kousseff syndrome
ORPHA:2351L1 syndrome
ORPHA:275543Larsen syndrome
ORPHA:503Laryngo-onycho-cutaneous syndrome
ORPHA:2407Laurin-Sandrow syndrome
ORPHA:2378Lethal ataxia with deafness and optic atrophy
ORPHA:1187Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466MASS syndrome
ORPHA:99715Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
ORPHA:83473Megalocornea-intellectual disability syndrome
ORPHA:2479Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Mixed connective tissue disease
ORPHA:809Mohr-Tranebjaerg syndrome
ORPHA:52368MOMO syndrome
ORPHA:2563Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Mosaic trisomy 8 syndrome
ORPHA:96061Multiple 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:623Neurogenic scapuloperoneal syndrome, Kaeser type
ORPHA:85146Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculodentodigital dysplasia
ORPHA:2710Oculofaciocardiodental syndrome
ORPHA:2712Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Oculotrichoanal syndrome
ORPHA:2717Onycho-tricho-dysplasia-neutropenia syndrome
ORPHA:2739Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 2
ORPHA:2751Otofaciocervical syndrome
ORPHA:2792