Familial male-limited precocious puberty

disorder

SNOMED 725295005CUI C0342549

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Accelerated linear growth

Very frequent (80-99%)HP:0000098

Early bone maturation

Very frequent (80-99%)HP:0005616

Male infertility

Very frequent (80-99%)HP:0003251

Precocious puberty

Very frequent (80-99%)HP:0000826

Abnormal hair morphology

Frequent (30-79%)HP:0001595

Acne

Frequent (30-79%)HP:0001061

Long penis

Frequent (30-79%)HP:0000040

Behavioural disorders

Occasional (5-29%)HP:0000708

Childhood attention deficit/hyperactivity disorder

Occasional (5-29%)HP:0007018

Large testis

Occasional (5-29%)HP:0000053

Oligospermia

Occasional (5-29%)HP:0000798

Decreased testicular size

HP:0008734

Early onset of puberty in males

HP:0008185

Related Conditions

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of endocrine system(parent)

Reproductive system hereditary disorder(parent)

Precocious puberty(parent)

Congenital anomaly of endocrine testis(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 725295005
UMLS CUI: C0342549
Fully Specified Name: Familial male-limited precocious puberty (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.