Agent Commons Collaborative Research

Leydig cell hypoplasia, type 1

rare

Any Leydig cell hypoplasia in which the cause of the disease is a mutation in the LHCGR gene.

Identifiers
MONDO:0009384 OMIM:238320
Causal genes
LHCGR
Part of
Leydig cell hypoplasiaHereditary disease
Also known as
Leydig cell hypoplasia caused by mutation in LHCGR · leydig cell hypoplasia with hypergonadotropic hypogonadism · leydig cell hypoplasia with pseudohermaphroditism · LHCGR Leydig cell hypoplasia

Subtypes

All diseases Rare only
Disease Subtypes
Leydig cell hypoplasia due to complete LH resistance
Leydig cell hypoplasia due to partial LH resistance

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