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"

64 matching diseasesClear search ×

Isolated proximal femoral focal deficiency

PFFD · CPFD

ORPHA:633228

Aromatase deficiency

Congenital estrogen deficiency

ORPHA:91

Ataxia with vitamin E deficiency

AVED · Ataxia with isolated vitamin E deficiency

ORPHA:96

Congenital deficiency in alpha-fetoprotein

ORPHA:168612

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 intrinsic factor deficiency

Congenital pernicious anemia · Gastric intrinsic factor deficiency

ORPHA:332

Congenital isolated ACTH deficiency

ORPHA:199296

Congenital lactase deficiency

ORPHA:53690

Congenital megaprepuce

Isolated congenital buried penis

ORPHA:696897

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

Familial hyperprolactinemia

Familial isolated prolactin receptor deficiency

ORPHA:397685

Hemophilia A

Congenital Factor VIII deficiency · Congenital F8 deficiency

ORPHA:98878

Hemophilia B

Congenital F9 deficiency · Christmas disease

ORPHA:98879

Isolated apodia

Isolated congenital absence of foot

ORPHA:294986

Isolated complex I deficiency

Isolated NADH-coenzyme Q reductase deficiency · Isolated NADH-ubiquinone reductase deficiency

ORPHA:2609

Isolated complex III deficiency

Isolated CoQ-cytochrome C reductase deficiency · Isolated coenzyme Q-cytochrome C reductase deficiency

ORPHA:1460

Isolated congenital aglossia

ORPHA:563951

Isolated congenital alacrima

ORPHA:91416

Isolated congenital anonychia

Isolated anonychia

ORPHA:79143

Isolated congenital anosmia

ORPHA:88620

Isolated congenital breast hypoplasia/aplasia

Isolated congenital amastia

ORPHA:180188

Isolated congenital ectropion

ORPHA:99171

Isolated congenital entropion

ORPHA:519386

Isolated congenital femoral bifurcation

Isolated congenital distal femoral duplication

ORPHA:667589

Isolated congenital hypogonadotropic hypogonadism

Isolated congenital gonadotropin deficiency · Gonadotropic deficiency

ORPHA:238666

Isolated congenital syngnathia

Isolated congenital maxillomandibular fusion

ORPHA:141214

Isolated cytochrome C oxidase deficiency

Isolated COX deficiency · Isolated mitochondrial respiratory chain complex IV deficiency

ORPHA:254905

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 follicle stimulating hormone deficiency

Isolated FSH deficiency

ORPHA:52901

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 nail clubbing

Isolated congenital acropachy · Isolated congenital digital clubbing

ORPHA:217059