About: familial male-limited precocious puberty

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease endocrine system disease nodeID://b50945024
label	familial male-limited precocious puberty
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111545
database_cross_reference	GARD:4475 MESH:C536961 MESH:D011629 OMIM:176410 ORDO:3000 SNOMEDCT_US_2021_09_01:237818003 UMLS_CUI:C0342549 UMLS_CUI:C1504412
has_exact_synonym	FMPP (en) male-limited precocious puberty (en) testotoxicosis (en) familial gonadotropin-independent male-limited sexual precocity (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	An endocrine system disease characterized by onset in early childhood of accelerated growth, early development of secondary sexual characteristics, and reduced adult height in males only that has_material_basis_in heterozygous mutation in LHCGR on chromosome 2p16.3.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50945025

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