Congenital contractural arachnodactyly
ORPHA:115Congenital insensitivity to pain syndrome, Marsili type
ORPHA:653728Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
ORPHA:1875Corneodermatoosseous syndrome
ORPHA:3194CPE-related Prader-Willi-like syndrome
ORPHA:633028Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome
ORPHA:171839Cutis verticis gyrata-intellectual disability syndrome
ORPHA:1557Deafness-intellectual disability syndrome, Martin-Probst type
ORPHA:85321Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome
ORPHA:3038Diencephalic syndrome
ORPHA:1672Diethylstilbestrol syndrome
ORPHA:1916Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
ORPHA:2229Distal deletion 3p syndrome
ORPHA:1620Ectrodactyly-cleft palate syndrome
ORPHA:1889EEM syndrome
ORPHA:1897Endocrine-cerebro-osteodysplasia syndrome
ORPHA:199332Epidermolysis bullosa simplex with anodontia/hypodontia
ORPHA:2325Erythrokeratodermia-cardiomyopathy syndrome
ORPHA:476096Familial atypical multiple mole melanoma syndrome
ORPHA:404560Feingold syndrome
ORPHA:1305Fibrodysplasia ossificans progressiva
ORPHA:337Fibrous dysplasia/McCune-Albright syndrome
ORPHA:595216Focal facial dermal dysplasia type I
ORPHA:79133GMS syndrome
ORPHA:2090Gorlin syndrome
ORPHA:377Gorlin-Chaudhry-Moss syndrome
ORPHA:2095H syndrome
ORPHA:168569Hearing loss-familial salivary gland insensitivity to aldosterone syndrome
ORPHA:3225HEC syndrome
ORPHA:2119HELLP syndrome
ORPHA:244242Hyperphosphatasia-intellectual disability syndrome
ORPHA:247262Hypocomplementemic urticarial vasculitis
ORPHA:36412Hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
ORPHA:88637IBIDS syndrome
ORPHA:453Intellectual disability-early-onset cataract-microcephaly syndrome
ORPHA:633035Intellectual disability-obesity-prognathism-eye and skin anomalies syndrome
ORPHA:397973ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement
ORPHA:457375Juberg-Marsidi syndrome
ORPHA:93972KID syndrome
ORPHA:477Kjellin syndrome
ORPHA:100996L1 syndrome
ORPHA:275543Lethal ataxia with deafness and optic atrophy
ORPHA:1187Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome
ORPHA:1816Limb-mammary syndrome
ORPHA:69085Lung agenesis-heart defect-thumb anomalies syndrome
ORPHA:1120Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
ORPHA:457485Maffucci syndrome
ORPHA:163634MAGIC syndrome
ORPHA:324972