Hypertelorism-microtia-facial clefting syndrome
ORPHA:2213Hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome
ORPHA:1882Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637Hypoparathyroidism-sensorineural deafness-renal disease syndrome
ORPHA:2237Hypospadias-intellectual disability, Goldblatt type syndrome
ORPHA:2261IBIDS syndrome
ORPHA:453ICF syndrome
ORPHA:2268Ichthyosis-hypotrichosis syndrome
ORPHA:91132Iridocorneal endothelial syndrome
ORPHA:64734JMP syndrome
ORPHA:324999Joubert syndrome with hepatic defect
ORPHA:1454Juberg-Hayward syndrome
ORPHA:2319Juberg-Marsidi syndrome
ORPHA:93972KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Lambert syndrome
ORPHA:1296Laryngo-onycho-cutaneous syndrome
ORPHA:2407Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816LIG4 syndrome
ORPHA:99812Lower limb malformation-hypospadias syndrome
ORPHA:2487Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649MASS syndrome
ORPHA:99715Mayer-Rokitansky-Küster-Hauser syndrome
ORPHA:3109Megacystis-microcolon-intestinal hypoperistalsis syndrome
ORPHA:2241Megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
ORPHA:83473Megalocornea-intellectual disability syndrome
ORPHA:2479Metaphyseal chondrodysplasia, Rosenberg type
ORPHA:1837Microphthalmia with linear skin defects syndrome
ORPHA:2556MOMO syndrome
ORPHA:2563Monosomy 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:623Nevo syndrome
ORPHA:2691Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972NPHP3-related Meckel-like syndrome
ORPHA:3032Oculodentodigital dysplasia
ORPHA:2710Oculofaciocardiodental syndrome
ORPHA:2712Oculogastrointestinal-neurodevelopmental syndrome
ORPHA:611201