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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"
Midline interhemispheric variant of holoprosencephaly
MIH · MIH type HPE
Hemihyperplasia-multiple lipomatosis syndrome
HHML
Hypoinsulinemic hypoglycemia and body hemihypertrophy
Isolated hemihyperplasia
Hemi 3 syndrome · Hemicorporal hypertrophy
OBSOLETE: Hemihypertrophy-intestinal web-corneal opacity syndrome
OBSOLETE: HIPO syndrome