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"

49 matching diseasesClear search ×

Moderate hemophilia B

Moderate congenital F9 deficiency · Moderate congenital factor IX deficiency

ORPHA:169796

Aromatase deficiency

Congenital estrogen deficiency

ORPHA:91

Congenital alpha2-antiplasmin deficiency

ORPHA:79

Congenital deficiency in alpha-fetoprotein

ORPHA:168612

Congenital enterocyte heparan sulfate deficiency

ORPHA:103910

Congenital enteropathy due to enteropeptidase deficiency

Congenital enterokinase deficiency

ORPHA:168601

Congenital factor II deficiency

Dysprothrombinemia · Hypoprothrombinemia

ORPHA:325

Congenital factor V deficiency

Owren disease · Parahemophilia

ORPHA:326

Congenital factor VII deficiency

Congenital proconvertin deficiency · Hypoproconvertinemia

ORPHA:327

Congenital factor X deficiency

Congenital Stuart factor deficiency · Stuart-Prower factor deficiency

ORPHA:328

Congenital factor XI deficiency

Hemophilia C · PTA deficiency

ORPHA:329

Congenital factor XII deficiency

Congenital Hageman factor deficiency

ORPHA:330

Congenital factor XIII deficiency

Fibrin-stabilizing factor deficiency

ORPHA:331

Congenital fibrinogen deficiency

ORPHA:335

Congenital high-molecular-weight kininogen deficiency

ORPHA:483

Congenital hyperinsulinism due to HNF4A deficiency

Hyperinsulinemic hypoglycemia due to HNF4A deficiency

ORPHA:263455

Congenital intrinsic factor deficiency

Congenital pernicious anemia · Gastric intrinsic factor deficiency

ORPHA:332

Congenital isolated ACTH deficiency

ORPHA:199296

Congenital lactase deficiency

ORPHA:53690

Congenital muscular dystrophy with integrin alpha-7 deficiency

Congenital muscular dystrophy with ITGA7 deficiency

ORPHA:34520

Congenital neutropenia-combined immunodeficiency due to MKL1 deficiency

MKL1-related neutrophil motility defect · Congenital neutropenia-combined immunodeficiency due to Megakaryoblastic leukemia 1 deficiency

ORPHA:619941

Congenital plasminogen activator inhibitor type 1 deficiency

Congenital PAI-1 deficiency

ORPHA:465

Congenital prekallikrein deficiency

ORPHA:749

Congenital sucrase-isomaltase deficiency

CSID · Congenital sucrose intolerance

ORPHA:35122

Congenital thrombotic thrombocytopenic purpura

Congenital ADAMTS-13 deficiency · Congenital TTP

ORPHA:93583

Congenital vertebral-cardiac-renal anomalies syndrome

Congenital NAD deficiency disorder

ORPHA:521438

Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

Glycogen storage disease type IV, congenital neuromuscular form · Glycogenosis type IV, congenital neuromuscular form

ORPHA:308670

Hemophilia A

Congenital Factor VIII deficiency · Congenital F8 deficiency

ORPHA:98878

Hemophilia B

Congenital F9 deficiency · Christmas disease

ORPHA:98879

Isolated congenital hypogonadotropic hypogonadism

Isolated congenital gonadotropin deficiency · Gonadotropic deficiency

ORPHA:238666

Isolated femoral agenesis/hypoplasia

Isolated congenital femoral deficiency · Isolated congenital short femur

ORPHA:1987

Isolated fibular hemimelia

Isolated congenital longitudinal deficiency of the fibula · Isolated fibular longitudinal meromelia

ORPHA:93323

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

Isolated humeral agenesis/hypoplasia

Isolated humeral intercalary meromelia · Isolated congenital absence of humerus

ORPHA:294973

Isolated proximal femoral focal deficiency

PFFD · CPFD

ORPHA:633228

Isolated tibial hemimelia

Isolated congenital absence of tibia · Isolated congenital aplasia and dysplasia of the tibia with intact fibula

ORPHA:93322

Isolated ulnar hemimelia

Isolated ulnar deficiency of forearm · Isolated ulnar longitudinal meromelia

ORPHA:93320

Mild hemophilia A

Mild congenital factor VIII deficiency · Mild congenital F8 deficiency

ORPHA:169808

Mild hemophilia B

Mild congenital factor IX deficiency · Mild congenital F9 deficiency

ORPHA:169799

Moderate hemophilia A

Moderate congenital factor VIII deficiency · Moderate congenital F8 deficiency

ORPHA:169805

Neurodegenerative syndrome due to cerebral folate transport deficiency

Folate receptor alpha deficiency · Cerebral folate transport deficiency

ORPHA:217382

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

Obesity due to congenital leptin deficiency

ORPHA:66628

Severe hemophilia A

Severe congenital factor VIII deficiency · Severe congenital F8 deficiency

ORPHA:169802