Kallmann syndrome

E2207153 UNEXPLORED

Kallmann syndrome is a rare genetic disorder characterized by delayed or absent puberty and an impaired sense of smell due to deficient production of certain hormones in the brain.

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All labels observed (1)

Label	Occurrences
Kallmann syndrome canonical	1

Referenced by (1)

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

Jimmy Scott → medicalCondition → Kallmann syndrome ⓘ