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MIM:600092 - NIVELON-NIVELON-MABILLE SYNDROME; NNMS
Xenbase Genes:
Human Disease Resource: MIM
MONDO:0010814 - chondrodysplasia-pseudohermaphroditism syndrome |
DOID:0060644 - chondrodysplasia-pseudohermaphroditism syndrome |
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MONDO:0010814 - chondrodysplasia-pseudohermaphroditism syndrome |
DOID:0060644 - chondrodysplasia-pseudohermaphroditism syndrome |