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MIM:615636 - JOUBERT SYNDROME 21; JBTS21
Xenbase Genes: cspp1
Human Disease Resource: MIM
MONDO:0014288 - Joubert syndrome 21 |
MONDO:0018342 - Joubert syndrome with Jeune asphyxiating thoracic dystrophy |
MONDO:0018772 - Joubert syndrome |
DOID:0110990 - Joubert syndrome 21 |