Isolated follicle stimulating hormone deficiency

disorder

SNOMED 758664007CUI C1856716

Overview

Isolated follicle stimulating hormone deficiency is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Decreased function of male gonad

Always present (100%)HP:0000026

Female hypogonadism

Always present (100%)HP:0000134

Pituitary gonadotropin deficiency

Always present (100%)HP:0008213

Decreased serum estradiol

Very frequent (80-99%)HP:0008214

Decreased sexual hair

Very frequent (80-99%)HP:0002225

Decreased testicular size

Very frequent (80-99%)HP:0008734

Decreased testosterone

Very frequent (80-99%)HP:0040171

Delayed menarche

Very frequent (80-99%)HP:0012569

Delayed puberty

Very frequent (80-99%)HP:0000823

Low gonadotropins (secondary hypogonadism)

Very frequent (80-99%)HP:0000044

Primary amenorrhea

Very frequent (80-99%)HP:0000786

Retarded ossification

Very frequent (80-99%)HP:0002750

Sparse axillary and pubic hair

Very frequent (80-99%)HP:0002215

Azoospermia

Frequent (30-79%)HP:0000027

Decreased female sex drive

Frequent (30-79%)HP:0030018

Hyperplasia of the Leydig cells

Frequent (30-79%)HP:0010791

Light or infrequent menstrual periods

Frequent (30-79%)HP:0000876

Oligospermia

Frequent (30-79%)HP:0000798

Teratozoospermia

Frequent (30-79%)HP:0012864

Testicular degeneration

Frequent (30-79%)HP:0000029

Two underdeveloped breasts

Frequent (30-79%)HP:0012814

Related Conditions

Isolated gonadotropin deficiency(parent)

Recessive hereditary disorder (autosomal)(parent)

Follicle stimulating hormone deficiency(parent)

Hereditary disorder of endocrine system(parent)

Hereditary disorder of nervous system(parent)

Congenital disease(parent)

Quick Facts

SNOMED CT: 758664007
UMLS CUI: C1856716
Fully Specified Name: Isolated follicle stimulating hormone deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 21

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.