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"

31 matching diseasesClear search ×

Isolated thyrotropin-releasing hormone deficiency

Isolated TRF deficiency · Isolated TRH deficiency

ORPHA:238670

Ataxia with vitamin E deficiency

AVED · Ataxia with isolated vitamin E deficiency

ORPHA:96

Congenital brain dysgenesis due to glutamine synthetase deficiency

Inherited GS deficiency · Inherited glutamine synthetase deficiency

ORPHA:71278

Congenital isolated ACTH deficiency

ORPHA:199296

Familial hyperprolactinemia

Familial isolated prolactin receptor deficiency

ORPHA:397685

Isolated ATP synthase deficiency

Isolated mitochondrial respiratory chain complex V deficiency

ORPHA:254913

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 hypogonadotropic hypogonadism

Isolated congenital gonadotropin deficiency · Gonadotropic deficiency

ORPHA:238666

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 glycerol kinase deficiency

Hyperglycerolemia

ORPHA:408

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 growth hormone deficiency type IV

ORPHA:684247

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 sedoheptulokinase deficiency

Isolated SHPK deficiency

ORPHA:440713

Isolated succinate-CoQ reductase deficiency

Isolated mitochondrial respiratory chain complex II deficiency · Isolated succinate-coenzyme Q reductase deficiency

ORPHA:3208

Isolated sulfite oxidase deficiency

ISOD · Sulfocysteinuria

ORPHA:99731

Isolated thyroid-stimulating hormone deficiency

Isolated thyrotropin deficiency · Isolated TSH deficiency

ORPHA:90674

Isolated ulnar hemimelia

Isolated ulnar deficiency of forearm · Isolated ulnar longitudinal meromelia

ORPHA:93320

Late-onset isolated ACTH deficiency

ORPHA:199299

Multiple mitochondrial dysfunctions syndrome type 5

ISCA1 deficiency · MMDS5

ORPHA:569274

Non-acquired isolated growth hormone deficiency

Congenital IGHD · Congenital isolated GH deficiency

ORPHA:631

Pseudo-Zellweger syndrome

Thiolase deficiency

ORPHA:2981

Recurrent infections associated with rare immunoglobulin isotypes deficiency

IgG subclass deficiency with IgA subclass deficiency · Isolated IgG subclass deficiency

ORPHA:183675