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"

131 matching diseasesClear search ×

FG syndrome type 1

Opitz-Kaveggia syndrome

ORPHA:93932

Griscelli syndrome type 1

Griscelli-Pruniéras syndrome type 1 · Hypopigmentation-neurologic impairment syndrome

ORPHA:79476

Griscelli syndrome type 2

Griscelli-Pruniéras syndrome type 2 · Hypopigmentation-immunodeficiency with or without neurologic impairment syndrome

ORPHA:79477

Griscelli syndrome type 3

Griscelli-Pruniéras syndrome type 3

ORPHA:79478

Heart-hand syndrome type 2

Atriodigital dysplasia type 2 · Tabatznik syndrome

ORPHA:1350

Heart-hand syndrome type 3

Atriodigital dysplasia type 3 · Cardiomelic syndrome type 3

ORPHA:1342

Hermansky-Pudlak syndrome due to AP3B1 deficiency

Hermansky-Pudlak syndrome due to adaptator related protein complex 3 subunit beta1 deficiency · Hermansky-Pudlak syndrome with neutropenia due to AP3B1 deficiency

ORPHA:664500

Holt-Oram syndrome

Atriodigital dysplasia type 1 · HOS

ORPHA:392

Hyper-IgM syndrome type 2

AID deficiency · Activation-induced cytidine deaminase deficiency

ORPHA:101089

Hyper-IgM syndrome type 3

HIGM3 · Hyper-IgM syndrome due to CD40 deficiency

ORPHA:101090

Hyper-IgM syndrome type 4

HIGM4

ORPHA:101091

Hyper-IgM syndrome type 5

HIGM5 · Hyper-IgM syndrome due to UNG deficiency

ORPHA:101092

IBIDS syndrome

Tay syndrome · Trichothiodystrophy type E

ORPHA:453

Immunodeficiency by defective expression of MHC class II

MHC class II deficiency · Bare lymphocyte syndrome type 2

ORPHA:572

Isolated Joubert syndrome

CPD IV · Cerebelloparenchymal disorder IV

ORPHA:475

Leukocyte adhesion deficiency type II

CDG syndrome type IIc · CDG-IIc

ORPHA:99843

Macrocephaly-congenital heart disease-facial dysmorphism-intellectual disability syndrome

Nabais Sa-de Vries type 2 syndrome

ORPHA:662175

Malan overgrowth syndrome

Sotos syndrome 2

ORPHA:420179

Marfan syndrome type 1

MFS1

ORPHA:284963

Marfan syndrome type 2

MFS2

ORPHA:284973

Marfanoid syndrome, De Silva type

ORPHA:2464

Mayer-Rokitansky-Küster-Hauser syndrome type 1

Congenital absence of uterus and vagina · MRKH syndrome type 1

ORPHA:247775

Mayer-Rokitansky-Küster-Hauser syndrome type 2

Atypical MRKH syndrome · MRKH syndrome type 2

ORPHA:2578

MGAT2-CDG

CDG syndrome type IIa · CDG-IIa

ORPHA:79329

Microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome

Houge-Janssens syndrome type 2

ORPHA:457284

Microcephaly-microcornea syndrome, Seemanova type

Seemanova-Lesny syndrome

ORPHA:2528

MOGS-CDG

CDG syndrome type IIb · CDG-IIb

ORPHA:79330

Monosomy 18p syndrome

18p- syndrome · De Grouchy syndrome type 1

ORPHA:1598

Monosomy 18q syndrome

18q- syndrome · Deletion 18q

ORPHA:1600

MPDU1-CDG

CDG syndrome type If · CDG-If

ORPHA:79323

MPI-CDG

CDG syndrome type Ib · CDG-Ib

ORPHA:79319

Mucopolysaccharidosis type 2, attenuated form

Hunter syndrome type B · Iduronate 2-sulfatase deficiency type B

ORPHA:217093

Mucopolysaccharidosis type 2, severe form

Hunter syndrome type A · Iduronate 2-sulfatase deficiency type A

ORPHA:217085

NPHP3-related Meckel-like syndrome

Goldston syndrome · Meckel syndrome type 7

ORPHA:3032

Orofaciodigital syndrome type 2

Mohr syndrome · OFD2

ORPHA:2751

Otopalatodigital syndrome type 2

OPD II syndrome · OPD syndrome 2

ORPHA:90652

Peeling skin syndrome type A

Generalized peeling skin syndrome type A · Non-inflammatory generalized peeling skin syndrome type A.

ORPHA:263548

Peeling skin syndrome type B

Generalized peeling skin syndrome type B · Inflammatory peeling skin syndrome

ORPHA:263553

Perrault syndrome type 1

XX gonadal dysgenesis-deafness syndrome-without neurological manifestations

ORPHA:642945

Perrault syndrome type 2

XX gonadal dysgenesis-deafness syndrome-progressive neurological manifestations

ORPHA:642976

Pfeiffer syndrome type 1

Classic Pfeiffer syndrome

ORPHA:93258

Pfeiffer syndrome type 2

ORPHA:93259

Pfeiffer syndrome type 3

ORPHA:93260

PGM1-CDG

CDG syndrome type It · CDG-It

ORPHA:319646

PHACE syndrome

Pascual-Castroviejo syndrome type 2 · PHACES syndrome

ORPHA:42775

PMM2-CDG

CDG syndrome type Ia · CDG-Ia

ORPHA:79318

Port-wine nevi-mega cisterna magna-hydrocephalus syndrome

Nova syndrome

ORPHA:2703

Progeroid syndrome, Petty type

Petty syndrome · Petty-Laxova-Wiedemann syndrome

ORPHA:2963