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Idiopathic central precocious puberty
1 associated gene
15 connected diseases
No signs/symptoms info
Disease Type of connection
16q24.3 microdeletion syndrome
Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis
Autosomal dominant Charcot-Marie-Tooth disease type 2P
Autosomal dominant nonsyndromic intellectual deficit
Autosomal recessive ataxia due to PEX10 deficiency
Autosomal recessive spastic paraplegia type 30
Dedifferentiated liposarcoma
Hereditary sensory and autonomic neuropathy type 2
Hydranencephaly
Infantile Refsum disease
KBG syndrome
Microlissencephaly
Neonatal adrenoleukodystrophy
Well-differentiated liposarcoma
Zellweger syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare gynecologic or obstetric disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
MKRN3 Q13064603856
No signs/symptoms info available.