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"

50 matching diseasesClear search ×

Congenital temporomandibular joint ankylosis

Congenital trismus

ORPHA:210576

Amniotic band syndrome

Congenital constriction ring syndrome · Congenital ring constrictions

ORPHA:295000

Congenital abducens nerve palsy

Benign congenital sixth cranial nerve palsy · Congenital CNVI palsy

ORPHA:440233

Congenital achiasma

ORPHA:324353

Congenital alacrima

ORPHA:98604

Congenital amyoplasia

Amyoplasia congenita

ORPHA:488586

Congenital chylothorax

ORPHA:264688

Congenital cornea plana

ORPHA:53691

Congenital cystic eye

Congenital anophthalmos with cyst

ORPHA:519384

Congenital ectropion

ORPHA:98570

Congenital epulis

Congenital gingival cell tumor · Congenital granular cell tumor

ORPHA:157826

Congenital genu flexum

ORPHA:295232

Congenital glaucoma

Buphthalmia · Buphthalmos

ORPHA:98976

Congenital heart block

Congenital atrioventricular block

ORPHA:60041

Congenital hemangioma

ORPHA:458775

Congenital hydrocephalus

ORPHA:2185

Congenital hypothyroidism

ORPHA:442

Congenital laryngeal cyst

ORPHA:141124

Congenital long QT syndrome

Congenital LQTS

ORPHA:768

Congenital megaprepuce

Isolated congenital buried penis

ORPHA:696897

Congenital microcoria

Congenital miosis

ORPHA:566

Congenital microgastria

ORPHA:199293

Congenital myopathy

ORPHA:97245

Congenital myotonia

ORPHA:206973

Congenital neutropenia

Constitutional neutropenia

ORPHA:101987

Congenital oculomotor nerve palsy

Congenital CNIII lesion · Congenital third cranial nerve palsy

ORPHA:440221

Congenital pancreatic cyst

Neonatal congenital pancreatic cyst · True congenital pancreatic cyst

ORPHA:313906

Congenital ptosis

ORPHA:91411

Congenital pulmonary vein atresia

Congenital PVA · CPVA

ORPHA:99126

Congenital short QT syndrome

Congenital SQTS

ORPHA:51083

Congenital syphilis

Mother-to-child transmission of syphilis · MTCT of syphilis

ORPHA:499009

Congenital thrombotic thrombocytopenic purpura

Congenital ADAMTS-13 deficiency · Congenital TTP

ORPHA:93583

Congenital toxoplasmosis

Toxoplasma embryofetopathy · Toxoplasma embryopathy

ORPHA:858

Congenital tracheal stenosis

ORPHA:141127

Congenital tracheomalacia

Congenital major airway collapse

ORPHA:95430

Congenital tricuspid malformation

ORPHA:98721

Congenital tricuspid stenosis

ORPHA:95459

Congenital trigeminal anesthesia

ORPHA:231013

Congenital trochlear nerve palsy

Congenital superior oblique palsy · Congenital CNIV palsy

ORPHA:98686

Congenital vertical talus

Congenital convex foot · Congenital convex pes valgus

ORPHA:178382

Diamond-Blackfan anemia

Diamond-Blackfan anemia syndrome · Congenital PRCA

ORPHA:124

Hereditary pulmonary alveolar proteinosis

Congenital PAP · Congenital pulmonary alveolar proteinosis

ORPHA:264675

Isolated growth hormone deficiency type IA

Congenital IGHD type IA · Congenital isolated GH deficiency type IA

ORPHA:231662

Isolated growth hormone deficiency type IB

Congenital IGHD type IB · Congenital isolated GH deficiency type IB

ORPHA:231671

Isolated growth hormone deficiency type II

Congenital IGHD type II · Congenital isolated GH deficiency type II

ORPHA:231679

Isolated growth hormone deficiency type III

Congenital IGHD type III · Congenital isolated GH deficiency type III

ORPHA:231692

Non-acquired combined pituitary hormone deficiency

Congenital combined pituitary hormone deficiency · Congenital hypopituitarism

ORPHA:467

Non-acquired isolated growth hormone deficiency

Congenital IGHD · Congenital isolated GH deficiency

ORPHA:631