Hypodontia-dysplasia of nails syndrome
ORPHA:2228Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome
ORPHA:363523Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Imperforate oropharynx-costovertebral anomalies syndrome
ORPHA:2759Iridocorneal endothelial syndrome
ORPHA:64734Isaacs syndrome
ORPHA:84142Jacobsen syndrome
ORPHA:2308JMP syndrome
ORPHA:324999Joubert syndrome with oculorenal defect
ORPHA:2318KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Larsen syndrome
ORPHA:503Laryngo-onycho-cutaneous syndrome
ORPHA:2407Laurin-Sandrow syndrome
ORPHA:2378Lethal ataxia with deafness and optic atrophy
ORPHA:1187LIG4 syndrome
ORPHA:99812Loose anagen syndrome
ORPHA:168Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASS syndrome
ORPHA:99715Maxillonasal dysplasia
ORPHA:1248Megalocornea-intellectual disability syndrome
ORPHA:2479Microphthalmia with linear skin defects syndrome
ORPHA:2556Monosomy 18p syndrome
ORPHA:1598Monosomy 18q syndrome
ORPHA:1600Monosomy 9p syndrome
ORPHA:261112Multiple 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:623Neuroectodermal-endocrine syndrome
ORPHA:2676Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201Oculotrichoanal syndrome
ORPHA:2717Odontomatosis-aortae esophagus stenosis syndrome
ORPHA:2724Ogden syndrome
ORPHA:276432Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Orofaciodigital syndrome type 2
ORPHA:2751