Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome
ORPHA:528105Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237Hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome
ORPHA:307936IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Ichthyosis follicularis-alopecia-photophobia syndrome
ORPHA:2273Infantile-onset spinocerebellar ataxia
ORPHA:1186Iridocorneal endothelial syndrome
ORPHA:64734Isolated hemihyperplasia
ORPHA:2128JMP syndrome
ORPHA:324999KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Laurin-Sandrow syndrome
ORPHA:2378LIG4 syndrome
ORPHA:99812Limb body wall complex
ORPHA:2369Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASS syndrome
ORPHA:99715Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megalocornea-intellectual disability syndrome
ORPHA:2479Melorheostosis with osteopoikilosis
ORPHA:1879Microphthalmia with linear skin defects syndrome
ORPHA:2556MOMO syndrome
ORPHA:2563Monosomy 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:623Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Null syndrome
ORPHA:280234OBSOLETE: Ito hypomelanosis
ORPHA:435Ocular anomalies-axonal neuropathy-developmental delay syndrome
ORPHA:496790Oculofaciocardiodental syndrome
ORPHA:2712Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Oguchi disease
ORPHA:75382Oley syndrome
ORPHA:79458