Isolated hemihyperplasia
ORPHA:2128JMP syndrome
ORPHA:324999Kabuki syndrome
ORPHA:2322Kahrizi syndrome
ORPHA:168972KAT6-related intellectual disability-craniofacial anomalies-cardiac defects syndrome
ORPHA:457193KBG syndrome
ORPHA:2332Keipert syndrome
ORPHA:2662Kenny-Caffey syndrome
ORPHA:2333Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
ORPHA:281201Keutel syndrome
ORPHA:85202Kindler epidermolysis bullosa
ORPHA:2908Kjellin syndrome
ORPHA:100996L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Laurin-Sandrow syndrome
ORPHA:2378Lethal ataxia with deafness and optic atrophy
ORPHA:1187LIG4 syndrome
ORPHA:99812Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASA syndrome
ORPHA:2466MASS syndrome
ORPHA:99715Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Michels syndrome
ORPHA:2506Microphthalmia with linear skin defects syndrome
ORPHA:2556Microphthalmia-brain atrophy syndrome
ORPHA:77299Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112MRCS syndrome
ORPHA:263347Mucopolysaccharidosis type 2
ORPHA:580Multiple 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:644Neurogenic scapuloperoneal syndrome, Kaeser type
ORPHA:85146Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Null syndrome
ORPHA:280234Oculodentodigital dysplasia
ORPHA:2710Oculofaciocardiodental syndrome
ORPHA:2712Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201