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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"
RIN2 syndrome
MACS syndrome · Macrocephaly-alopecia-cutis laxa-scoliosis syndrome
Achalasia-microcephaly syndrome
Cutis laxa-Marfanoid syndrome
Microcephaly-brachydactyly-kyphoscoliosis syndrome
Viljoen-Kallis-Voges syndrome
Radioulnar synostosis-microcephaly-scoliosis syndrome
Giuffré-Tsukahara syndrome · Tsukahara syndrome
Seizures-scoliosis-macrocephaly syndrome
SSM syndrome