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MORM syndrome
1 OMIM reference -
1 associated gene
2 connected diseases
No signs/symptoms info
Disease Type of connection
Joubert syndrome
Joubert syndrome with ocular defect
Synonym(s):
- Intellectual deficit - truncal obesity - retinal dystrophy - micropenis
- Mental retardation - truncal obesity - retinal dystrophy - micropenis
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare eye disease
- Rare genetic disease
Classification (ICD10):
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
1 MeSH reference: C536984
Gene symbol UniProt reference OMIM reference
INPP5E Q9NRR6613037
No signs/symptoms info available.