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 ×

Syndrome with congenital phagocyte functional defect as a major feature

Syndrome with congenital functional defect of phagocyte as a major feature · Syndrome with constitutional functional phagocyte defect as a major feature

ORPHA:674648

Congenital functional phagocyte defect

Congenital functional defect of phagocyte · Constitutional functional phagocyte defect

ORPHA:183681

Genetic syndrome with a central nervous system malformation as a major feature

Genetic syndrome with a CNS malformation as major feature

ORPHA:269564

Genetic syndrome with a cerebellar malformation as a major feature

ORPHA:269567

Genetic syndrome with a Dandy-Walker malformation as a major feature

ORPHA:269570

Genetic syndrome with corpus callosum agenesis/dysgenesis as a major feature

ORPHA:269573

Genetic syndrome with limb malformations as a major feature

ORPHA:404577

Non-syndromic congenital phagocyte functional defect

Non-syndromic constitutional functional phagocyte defect · Non-syndromic congenital functional defect of phagocytes

ORPHA:674896

Other syndrome with lissencephaly as a major feature

ORPHA:102010

Rare disease with adrenal Cushing syndrome as a major feature

ORPHA:314749

Syndrome with a central nervous system malformation as a major feature

ORPHA:108991

Syndrome with a cerebellar malformation as a major feature

ORPHA:269523

Syndrome with a Dandy-Walker malformation as a major feature

ORPHA:269546

Syndrome with alpha-thalassemia as a major feature

ORPHA:232288

Syndrome with congenital neutropenia as a major feature

Syndrome with constitutional neutropenia as a major feature · Syndrome with genetic neutropenia as a major feature

ORPHA:331184

Syndrome with corpus callosum agenesis/dysgenesis as a major feature

ORPHA:199639

Syndrome with limb malformations as a major feature

ORPHA:109009

Syndrome with microcephaly as a major feature

ORPHA:269528

Syndrome with pulmonary hypertension as a major feature

ORPHA:275853