Laron syndrome

E1767904 UNEXPLORED

Laron syndrome is a rare genetic disorder characterized by insensitivity to growth hormone, resulting in proportionate dwarfism and distinctive facial and metabolic features.

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All labels observed (1)

Label	Occurrences
Laron syndrome canonical	1

Referenced by (1)

Full triples — surface form annotated when it differs from this entity's canonical label.

Homo floresiensis → pathologyHypothesesConsidered → Laron syndrome ⓘ