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Familial atrial myxoma
1 OMIM reference -
1 associated gene
39 connected diseases
No signs/symptoms info
Disease Type of connection
Acrodysostosis
Acrodysostosis with multiple hormone resistance
Carney complex
Primary pigmented nodular adrenocortical disease
Retinitis pigmentosa
Williams syndrome
Periventricular nodular heterotopia
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Usher syndrome type 1
Giant cell glioblastoma
Gliosarcoma
Autosomal dominant nonsyndromic intellectual deficit
Acute myeloblastic leukemia with maturation
Acute myeloblastic leukemia without maturation
Acute myelomonocytic leukemia
Acute promyelocytic leukemia
Anophthalmia / microphthalmia - esophageal atresia
Classical homocystinuria
Colobomatous microphthalmia
Hereditary sensory and autonomic neuropathy type 2
Isolated anophthalmia - microphthalmia
Leber congenital amaurosis
Pigmented paravenous retinochoroidal atrophy
Pseudohypoaldosteronism type 2C
Pseudohypoaldosteronism type 2E
Septo-optic dysplasia
Chorioretinopathy, Birdshot type
Dedifferentiated liposarcoma
Familial melanoma
Well-differentiated liposarcoma
Blackfan-Diamond anemia
Early infantile epileptic encephalopathy
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Intellectual deficit, X-linked, Turner type
Multiple endocrine neoplasia type 1
Posterior polar cataract
Zollinger-Ellison syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C538262
Gene symbol UniProt reference OMIM reference
PRKAR1A P10644188830
No signs/symptoms info available.