Crandall syndrome
MONDO:0016067Mondo
Findings
No curated finding names Crandall syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
This syndrome is characterized by progressive sensorineural deafness, alopecia and hypogonadism with LH and GH deficiencies. It has been described in three brothers. It resembles Bjrnstad's syndrome that combines irregular pili torti and deafness. It is probably inherited as and autosomal recessive disorder.
Definition from the Mondo Disease Ontology (MONDO:0016067), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of
Other names
2 names
Resolves to: Crandall syndrome
- Also called
- alopecia-deafness-hypogonadism syndromealopecia-sensorineural deafness-hypogonadism syndrome