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"

105 matching diseasesClear search ×

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-myopathy-short stature-endocrine defect syndrome

Chudley-Rozdilsky syndrome

ORPHA:3068

Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome

Autosomal recessive intellectual disability due to TRAPPC9 deficiency

ORPHA:352530

Intellectual disability-seizures-macrocephaly-obesity syndrome

Der(8)t(8;12)

ORPHA:369950

Intellectual disability-strabismus syndrome

ORPHA:363528

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

Marfanoid habitus-autosomal recessive intellectual disability syndrome

Fragoso-Cantú syndrome

ORPHA:2463

Megalocornea-intellectual disability syndrome

MMR syndrome · Neuhäuser syndrome

ORPHA:2479

MEHMO syndrome

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

ORPHA:85282

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-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome

Microcephaly-intellectual disability-sensorineural deafness-epilepsy-abnormal muscle tone syndrome

ORPHA:457351

Microcephaly-lymphedema-chorioretinopathy syndrome

MLCRD

ORPHA:2526

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

Micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome

ORPHA:476126

Microphthalmia-ankyloblepharon-intellectual disability syndrome

MCOPS4 · Syndromic microphthalmia type 4

ORPHA:85275

Mirhosseini-Holmes-Walton syndrome

Pigmentary retinopathy-intellectual disability syndrome

ORPHA:3084

MOMO syndrome

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

ORPHA:2563

MORM syndrome

Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome

ORPHA:75858

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

ORPHA:3067

OBSOLETE: Intellectual disability-microcephaly-unusual facies syndrome

OBSOLETE: Thiele syndrome

ORPHA:3313

OBSOLETE: X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome

ORPHA:83648

Optic atrophy-intellectual disability syndrome

BBSOAS · Bosch-Boonstra-Schaaf optic atrophy syndrome

ORPHA:401777

Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome

Al Gazali-Nair syndrome

ORPHA:2773

Pinsky-Di George-Harley syndrome

Microphthalmia-intellectual disability syndrome

ORPHA:2895

Polyneuropathy-intellectual disability-acromicria-premature menopause syndrome

Lundberg syndrome

ORPHA:2928

Premature chromosome condensation with microcephaly and intellectual disability

ORPHA:52183

Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome

ORPHA:391408

Pseudo-TORCH syndrome type 1

Band like calcification with simplified gyration and polymicrogyria · BLC-PMG

ORPHA:1229

Rare genetic syndromic intellectual disability

ORPHA:183763

Rare non-syndromic intellectual disability

Rare NSID

ORPHA:101685

Rare syndromic intellectual disability

ORPHA:102369

Recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome

IDMDC

ORPHA:280384

Richieri Costa-da Silva syndrome

Myotonia-intellectual disability-skeletal anomalies syndrome

ORPHA:3101

SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome

ORPHA:597743

Severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome

IQSEC2-related syndromic intellectual disability

ORPHA:397933

Severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome

ORPHA:1236

SLC12A2-related autosomal recessive neonatal-developmental delay-intellectual disability-feeding difficulty-sensorineural deafness syndrome

Kilquist syndrome

ORPHA:633021