ADGRD2 gene related symptoms and diseases

All the information presented here about the ADGRD2 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE.

Top 5 symptoms associated to ADGRD2 gene



Symptoms // Phenotype % Cases
Autosomal dominant inheritance Very Common - Between 80% and 100% cases
Keratoconjunctivitis sicca Very Common - Between 80% and 100% cases
Conjunctival hyperemia Very Common - Between 80% and 100% cases
Hypopnea Very Common - Between 80% and 100% cases
Frontal balding Very Common - Between 80% and 100% cases

Other less frequent symptoms

Patients with ADGRD2 gene alterations may also develop some of the following symptoms and phenotypes:

Commonly - More than 50% cases

Increased reactive oxygen species production

Not very common - Between 30% and 50% cases

Enlarged polycystic ovaries

Commonly - More than 50% cases

Prostate cancer

Not very common - Between 30% and 50% cases

Abnormality of the ovary

Commonly - More than 50% cases

Menstrual irregularities

Not very common - Between 30% and 50% cases

Adrenal hyperplasia

Commonly - More than 50% cases

Obstructive sleep apnea

Not very common - Between 30% and 50% cases

Oligomenorrhea

And 19 more phenotypes.

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Rare diseases associated to ADGRD2 gene

Here you will find a list of rare diseases related to the ADGRD2. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


POLYCYSTIC OVARY SYNDROME 1; PCOS1

Alternate names

POLYCYSTIC OVARY SYNDROME 1; PCOS1 Is also known as pco1;pco, pcos, stein-leventhal syndrome, hyperandrogenemia

Description

a health problem that can affect a woman's menstrual cycle, fertility, hormones, insulin production, heart, blood vessels, and appearance

Most common symptoms of POLYCYSTIC OVARY SYNDROME 1; PCOS1

  • Autosomal dominant inheritance
  • Neoplasm
  • Abnormality of metabolism/homeostasis
  • Obesity
  • Diabetes mellitus


More info about POLYCYSTIC OVARY SYNDROME 1; PCOS1

SOURCES: UMLS ICD10 DOID COHD NCIT ICD9 SCTID MESH EFO MONDO OMIM



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