ICF syndrome
ORPHA:2268ICHAD syndrome
ORPHA:699599Ichthyosis follicularis-alopecia-photophobia syndrome
ORPHA:2273Ichthyosis-hypotrichosis syndrome
ORPHA:91132IMAGe syndrome
ORPHA:85173Infantile convulsions and choreoathetosis
ORPHA:31709Interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome
ORPHA:306504Inverted duplicated chromosome 15 syndrome
ORPHA:3306IRIDA syndrome
ORPHA:209981Iridocorneal endothelial syndrome
ORPHA:64734IRVAN syndrome
ORPHA:209943Isaacs syndrome
ORPHA:84142IVIC syndrome
ORPHA:2307JMP syndrome
ORPHA:324999Joubert syndrome with hepatic defect
ORPHA:1454Joubert syndrome with oculorenal defect
ORPHA:2318KBG syndrome
ORPHA:2332KID syndrome
ORPHA:477L1 syndrome
ORPHA:275543Laryngo-onycho-cutaneous syndrome
ORPHA:2407Lethal ataxia with deafness and optic atrophy
ORPHA:1187Mammary-digital-nail syndrome
ORPHA:238744Mandibular hypoplasia-deafness-progeroid features-lipodystrophy syndrome
ORPHA:363649Megalocornea-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:623Nodulosis-arthropathy-osteolysis syndrome
ORPHA:85196Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
ORPHA:363972Noonan syndrome-like disorder with loose anagen hair
ORPHA:2701Onycho-tricho-dysplasia-neutropenia syndrome
ORPHA:2739Ophthalmomandibulomelic dysplasia
ORPHA:2741Opsoclonus-myoclonus syndrome
ORPHA:1183Otofaciocervical syndrome
ORPHA:2792Otopalatodigital syndrome type 1
ORPHA:90650Otopalatodigital syndrome type 2
ORPHA:90652Pai syndrome
ORPHA:1993POEMS syndrome
ORPHA:2905Progressive supranuclear palsy
ORPHA:683Proteasome-associated autoinflammatory syndrome
ORPHA:324977