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"

47 matching diseasesClear search ×

Isolated nail clubbing

Isolated congenital acropachy · Isolated congenital digital clubbing

ORPHA:217059

Congenital isolated ACTH deficiency

ORPHA:199296

Congenital isolated hyperinsulinism

PHHI · Persistent hyperinsulinemic hypoglycemia of infancy

ORPHA:657

Congenital megaprepuce

Isolated congenital buried penis

ORPHA:696897

Familial congenital mirror movements

Familial congenital controlateral synkinesia · Hereditary congenital controlateral synkinesia

ORPHA:238722

Familial isolated congenital asplenia

ORPHA:101351

Isolated acheiria

Isolated congenital absence of hand

ORPHA:294983

Isolated amelia of lower limb

Isolated congenital absence of lower limb

ORPHA:294969

Isolated amelia of upper limb

Isolated congenital absence of upper limb

ORPHA:294967

Isolated apodia

Isolated congenital absence of foot

ORPHA:294986

Isolated congenital adermatoglyphia

Congenital absence of fingerprints · Immigration delay disease

ORPHA:289465

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 hepatic fibrosis

Isolated CHF

ORPHA:485426

Isolated congenital hypoglossia

ORPHA:563954

Isolated congenital hypoglossia/aglossia

ORPHA:141152

Isolated congenital hypogonadotropic hypogonadism

Isolated congenital gonadotropin deficiency · Gonadotropic deficiency

ORPHA:238666

Isolated congenital laryngeal web

ORPHA:2374

Isolated congenital megalocornea

Congenital anterior megalophthalmia

ORPHA:91489

Isolated congenital microcephaly

ORPHA:199642

Isolated congenital onychodysplasia

COIF · COIF syndrome

ORPHA:79144

Isolated congenital radial head dislocation

Isolated congenital elbow dislocation

ORPHA:295032

Isolated congenital sclerocornea

ORPHA:91490

Isolated congenital syngnathia

Isolated congenital maxillomandibular fusion

ORPHA:141214

Isolated femoral agenesis/hypoplasia

Isolated congenital femoral deficiency · Isolated congenital short femur

ORPHA:1987

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 humero-radial synostosis

Isolated congenital humeroradial fusion

ORPHA:3265

Isolated humero-ulnar synostosis

Isolated congenital humeroulnar fusion

ORPHA:94056

Isolated hyperphalangy

Supernumerary phalanx · Isolated congenital supernumerary phalanges

ORPHA:295002

Isolated hypoplasia of thumb

Isolated congenital thumb hypodactyly · Isolated congenital thumb oligodactyly

ORPHA:294988

Isolated proximal femoral focal deficiency

PFFD · CPFD

ORPHA:633228

Isolated pyloric duplication

Isolated duplication cyst of the pyloric canal · Isolated duplication cyst of the pylorus

ORPHA:662405

Isolated radio-ulnar synostosis

Isolated congenital radioulnar fusion

ORPHA:3269

Isolated tibial hemimelia

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

ORPHA:93322

Isolated tibio-fibular synostosis

Isolated congenital tibiofibular fusion

ORPHA:295028

Non-acquired isolated growth hormone deficiency

Congenital IGHD · Congenital isolated GH deficiency

ORPHA:631

T-cell immunodeficiency with thymic aplasia

Nezelof syndrome · Isolated congenital athymia

ORPHA:83471