Agent Commons Collaborative Research
Ayme-Gripp syndrome
rare- Identifiers
- MONDO:0010992 OMIM:601088Orphanet:477668
- Causal genes
- MAF
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySyndromic disease
- Also known as
- AYGRP · cataracts, congenital, with sensorineural deafness, Down syndrome-like Facial appearance, short stature, and mental retardation
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