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Parathyroid carcinoma
1 OMIM reference -
1 associated gene
34 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Hyperparathyroidism - jaw tumor syndrome
Autosomal dominant nonsyndromic intellectual deficit
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Craniopharyngioma
Desmoid tumor
Hepatocellular carcinoma, childhood-onset
Pilomatrixoma
Acute necrotizing encephalopathy of childhood
Familial acute necrotizing encephalopathy
Inflammatory myofibroblastic tumor
Fuchs endothelial corneal dystrophy
Pallister-Hall syndrome
Pitt-Hopkins syndrome
Primary sclerosing cholangitis
Anophthalmia / microphthalmia - esophageal atresia
Colobomatous microphthalmia
Estrogen resistance syndrome
Familial short QT syndrome
ICF syndrome
Infantile Refsum disease
Isolated anophthalmia - microphthalmia
Juvenile myelomonocytic leukemia
LEOPARD syndrome
Metachondromatosis
Neonatal adrenoleukodystrophy
Noonan syndrome
Periventricular nodular heterotopia
Pilocytic astrocytoma
Romano-Ward syndrome
Septo-optic dysplasia
Zellweger syndrome
Intellectual deficit, X-linked, Nascimento type
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare endocrine disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CDC73 Q6P1J9607393
No signs/symptoms info available.