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"

7 matching diseasesClear search ×

Midline interhemispheric variant of holoprosencephaly

MIH · MIH type HPE

ORPHA:93926

Aprosencephaly/atelencephaly spectrum

AP/AT spectum

ORPHA:566847

Atelencephaly

Atelencephalic microcephaly

ORPHA:566852

Iniencephaly

ORPHA:63259

Lissencephaly

ORPHA:48471

Porencephaly

ORPHA:2940

Schizencephaly

ORPHA:799