Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

138 matching diseasesClear search ×

HIDEA syndrome

Severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome

ORPHA:436141

Hyperphosphatasia-intellectual disability syndrome

Mabry syndrome

ORPHA:247262

Hypogonadism-mitral valve prolapse-intellectual disability syndrome

Cantalamessa-Baldini-Ambrosi syndrome

ORPHA:2233

Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome

Shaheen syndrome

ORPHA:363523

Hypospadias-intellectual disability, Goldblatt type syndrome

Goldblatt-Wallis syndrome

ORPHA:2261

Intellectual disability-alacrima-achalasia syndrome

ORPHA:289483

Intellectual disability-cupped ears syndrome

Snijders Blok-Fisher syndrome

ORPHA:656135

Intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome

ORPHA:3044

Intellectual disability-early-onset cataract-microcephaly syndrome

Baralle-Macken syndrome

ORPHA:633035

Intellectual disability-expressive aphasia-facial dysmorphism syndrome

SETBP1 haploinsufficiency disorder · Intellectual disability-loss of expressive language-facial dysmorphism syndrome

ORPHA:436151

Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome

CTNNB1-related neurodevelopmental disorder · CTNNB1-NDD

ORPHA:404473

Intellectual disability-facial dysmorphism-joint hypermobility-hearing loss syndrome

Beck-Fahrner syndrome · TET3-related Beck-Fahrner syndrome

ORPHA:684216

Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome

Da Silva syndrome

ORPHA:1495

Intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome

ORPHA:314575

Intellectual disability-hypotonia-facial dysmorphism-macrocephaly syndrome

KMT5B haploinsufficiency neurodevelopmental disorder

ORPHA:684226

Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome

PPP2R5D-related neurodevelopmental disorder · Houge-Janssens syndrome type 1

ORPHA:457279

Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome

MCAHS type 3 · Multiple congenital anomalies-hypotonia-seizures syndrome type 3

ORPHA:369837

Intellectual disability-seizures-macrocephaly-obesity syndrome

Der(8)t(8;12)

ORPHA:369950

Intellectual disability-short stature-hypertelorism syndrome

Stoll-Géraudel-Chauvin syndrome

ORPHA:3074

Intellectual disability-spasticity-ectrodactyly syndrome

Jancar syndrome

ORPHA:1891

Intellectual disability-strabismus syndrome

ORPHA:363528

KBG syndrome

Short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome · ANKRD11-related disorder

ORPHA:2332

Lambert syndrome

Branchial dysplasia-intellectual disability-inguinal hernia syndrome

ORPHA:1296

Macrocephaly-congenital heart disease-facial dysmorphism-intellectual disability syndrome

Nabais Sa-de Vries type 2 syndrome

ORPHA:662175

Macrocephaly-intellectual disability-autism syndrome

ORPHA:210548

Macrocephaly-intellectual disability-left ventricular non compaction syndrome

ORPHA:466791

Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome

Smith-Kingsmore syndrome · MINDS syndrome

ORPHA:457485

MAN1B1-CDG

Congenital disorder of glycosylation type 2 due to MAN1B1 deficiency · Congenital disorder of glycosylation type II due to MAN1B1 deficiency

ORPHA:397941

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

MEHMO syndrome

X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome

ORPHA:85282

Mesomelic dysplasia-digital anomalies-intellectual disability syndrome

ORPHA:632603

Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome

Microcephaly-cerebellar hypoplasia-congenital heart conduction defect syndrome

ORPHA:329332

Microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom

ORPHA:500159

Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome

Houge-Janssens syndrome type 2

ORPHA:457284

Microcephaly-corpus callosum hypoplasia-simplified gyral pattern-intellectual disability syndrome

DYNC1I2-related neurodevelopmental disorder

ORPHA:699844

Microcephaly-deafness-intellectual disability syndrome

Kawashima-Tsuji syndrome · Microcephaly-hearing loss-intellectual disability syndrome

ORPHA:2533

Microcephaly-digital anomalies-intellectual disability syndrome

Kelly-Kirson-Wyatt syndrome

ORPHA:137653

Microcephaly-hearing loss-facial dysmorphism-intellectual disability syndrome

Nabais Sa-de Vries type 1 syndrome · Microcephaly-deafness-facial dysmorphism-intellectual disability syndrome

ORPHA:662179

Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome

Woods-Crouchman-Huson syndrome

ORPHA:137658

Microcephaly-seizures-intellectual disability-heart disease syndrome

ORPHA:2519

Microcephaly-short stature-intellectual disability-facial dysmorphism syndrome

ORPHA:423306

Microcephaly-thin corpus callosum-intellectual disability syndrome

ORPHA:397951

Microphthalmia-ankyloblepharon-intellectual disability syndrome

MCOPS4 · Syndromic microphthalmia type 4

ORPHA:85275

MOMO syndrome

Macrocephaly-obesity-intellectual disability-ocular abnormalities syndrome · Macrosomia-obesity-macrocephaly-ocular abnormalities syndrome

ORPHA:2563

Mowat-Wilson syndrome

Hirschsprung disease-intellectual disability syndrome

ORPHA:2152

Nicolaides-Baraitser syndrome

Intellectual disability-sparse hair-brachydactyly syndrome

ORPHA:3051

OBSOLETE: Hirsutism-skeletal dysplasia-intellectual disability syndrome

OBSOLETE: Wiedemann-Oldigs-Oppermann syndrome

ORPHA:2156

OBSOLETE: Intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome

ORPHA:3067