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"

48 matching diseasesClear search ×

MYH9-related syndromic thrombocytopenia

MYH9-RD · MYH9-related disorder

ORPHA:182050

Alpha-thalassemia and related disorders

ORPHA:275745

Autosomal dominant intellectual disability-craniofacial dysmorphism-macrocephaly-hypotonia syndrome due to H1-4 mutation

H1-4-related neurodevelopmental disorder · Rahman syndrome

ORPHA:642763

Beta-thalassemia and related disorders

ORPHA:275749

Cataract-combined malonic and methylmalonic aciduria-intellectual disability syndrome

ZBTB11-related neurodevelopmental disorder

ORPHA:699835

CDK13-related developmental delay-intellectual disability-facial dysmorphism-congenital heart defects syndrome

CDK13-related disorder

ORPHA:646278

CHD4-related neurodevelopmental disorder

Sifrim-Hitz-Weiss syndrome · CHD4-related neurodevelopmental syndrome

ORPHA:653712

Common variable immunodeficiency and related disorders

CVID and related disorders

ORPHA:696851

Congenital disorder of glycosylation-related bone disorder

CDG-related bone disorder

ORPHA:371195

Congenital scalp aplasia cutis-enamel hypoplasia-developmental delay-intellectual disability syndrome

FOSL2-related neurodevelopmental disorder

ORPHA:697356

CTCF-related neurodevelopmental disorder

ORPHA:363611

Disorder of lysosomal-related organelles

ORPHA:309340

EEC syndrome and related disorders

EEC syndrome and related syndrome · Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome and related disorders

ORPHA:98609

Factor V short isoforms-related bleeding disorder

FV short isoforms-related bleeding disorder

ORPHA:599519

Filamin-related bone disorder

Bone filaminopathy

ORPHA:93425

Global developmental delay-intellectual disability-microcephaly-short stature-brain iron accumulation syndrome

Hengel-Maroofian-Schols syndrome · BCAS3-related neurodevelopmental disorder

ORPHA:697067

Global developmental delay-speech apraxia-facial dysmorphism-limb and palpebral anomalies syndrome

ZNF148-related neurodevelopmental disorder

ORPHA:708178

GNAO1-related developmental delay-seizures-movement disorder spectrum

GNAO1-related spectrum · GNAO1-related neurodevelopmental disorder

ORPHA:592564

GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder

GRIN2B-Related Neurodevelopmental Disorder

ORPHA:589547

Human herpesvirus 8-related disorder

HHV-8-related disorder

ORPHA:102024

Infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome

Baker-Gordon syndrome · SYT1-related neurodevelopmental disorder

ORPHA:522077

Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome

CTNNB1-related neurodevelopmental disorder · CTNNB1-NDD

ORPHA:404473

Intellectual disability-speech delay-dysmorphic features-T cell abnormalities syndrome

BCL11B-related neurodevelopmental disorder

ORPHA:662829

Joubert syndrome and related disorders

JSRD

ORPHA:140874

KAT6B-related multiple congenital anomalies syndrome

KAT6B-related disorder

ORPHA:597749

KBG syndrome

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

ORPHA:2332

Marfan syndrome and Marfan-related disorders

ORPHA:284993

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

DYNC1I2-related neurodevelopmental disorder

ORPHA:699844

Mixed dermis disorder

ORPHA:79380

Neurodevelopmental delay-brain malformations-skeletal defects-intellectual disability syndrome

Neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects · HNRPH1-related neurodevelopmental disorder

ORPHA:662207

Neurodevelopmental delay-congenital heart defects-intellectual disability syndrome

Radio-Tartaglia syndrome · SPEN-related neurodevelopmental disorder

ORPHA:662234

Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome

DHX30-related neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome · DHX30-related neurodevelopmental disorder

ORPHA:647788

Neurodevelopmental disorder-brain malformation-facial dysmorphism-brachydactyly syndrome

HNRNPR-related neurodevelopmental disorder

ORPHA:662189

Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome

Okamoto syndrome · HNRNPK-related neurodevelopmental disorder

ORPHA:453499

OBSOLETE: Aggrecan-related bone disorder

ORPHA:364817

OBSOLETE: Perlecan-related bone disorder

ORPHA:93424

Ophthalmological abnormalities-facial dysmorphism-intellectual disability syndrome

BRPF1-related neurodevelopmental disorder

ORPHA:698090

Osteopetrosis and related disorders

ORPHA:2781

Proteoglycan-related bone disorder

ORPHA:674499

Recessive KLHL7-related disorder

ORPHA:603699

Severe neurodevelopmental disorder-facial dysmorphism-cerebral-renal-cardiac anomalies syndrome

TM2D3-related neurodevelopmental disorder

ORPHA:708166

Spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder

SPOAN and SPOAN-related disorder

ORPHA:431320

Sulfation-related bone disorder

ORPHA:93423

Thrombomodulin-related bleeding disorder

THBD-related bleeding disorder · THBD-related coagulopathy

ORPHA:436169

TRPV4-related bone disorder

ORPHA:364820

Turnpenny-Fry syndrome

PCGF2-related disorder · TPFS

ORPHA:688642

Type 11 collagen-related bone disorder

ORPHA:93422

Type 2 collagen-related bone disorder

ORPHA:93421