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"

19 matching diseasesClear search ×

Pseudoaminopterin syndrome

ASSA · Aminopterin syndrome-like sine aminopterin

ORPHA:221120

Abruzzo-Erickson syndrome

CHARGE-like syndrome · Cleft palate-coloboma-deafness syndrome

ORPHA:921

Aminopterin/methotrexate embryofetopathy

Aminopterin embryopathy syndrome · Fetal aminopterin syndrome

ORPHA:1908

Autosomal recessive faciodigitogenital syndrome

Aarskog-like syndrome · Facio-digito-genital syndrome, Kuwait type

ORPHA:1974

Body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency

PXE-like syndrome · Pseudoxanthoma elasticum-like syndrome

ORPHA:91135

Bohring-Opitz syndrome

BOS syndrome · Bohring syndrome

ORPHA:97297

Congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome

Serpentine-like syndrome

ORPHA:514352

Fraser-like syndrome

ORPHA:2051

Isotretinoin-like syndrome

Kawashima syndrome · Microtia-aortic arch syndrome

ORPHA:2306

ITPA-related lethal infantile neurological disorder with cataract and cardiac involvement

Martsolf-like syndrome

ORPHA:457375

Laron syndrome with immunodeficiency

Laron-like syndrome · Short stature due to STAT5b deficiency

ORPHA:220465

Legius syndrome

Nonmosaic Legius syndrome · NF1-like syndrome

ORPHA:137605

Marin-Amat syndrome

ORPHA:101104

PEHO-like syndrome

ORPHA:99807

Proteus-like syndrome

ORPHA:2969

Robinow-like syndrome

Saal-Greenstein syndrome

ORPHA:3105

Spastic paraplegia-intellectual disability-nystagmus-obesity syndrome

SINO syndrome

ORPHA:521390

Weaver-like syndrome

ORPHA:3446

Wolfram-like syndrome

ORPHA:411590