progeroid syndrome, Petty type
human disease
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progeroid syndrome, Petty type
Summary
progeroid syndrome, Petty type is a developmental defect during embryogenesis[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- progeroid syndrome, Petty type's instance of is recorded as developmental defect during embryogenesis[3].
- progeroid syndrome, Petty type's instance of is recorded as class of disease[4].
- progeroid syndrome, Petty type is a type of progeroid syndrome[5].
- progeroid syndrome, Petty type's genetic association is recorded as SLC25A24[6].
- progeroid syndrome, Petty type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2963[7].
Why It Matters
progeroid syndrome, Petty type is known by 8 alternative names across languages and contexts.[2]