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Microlissencephaly
1 OMIM reference -
1 associated gene
17 connected diseases
No signs/symptoms info
Disease Type of connection
Hydranencephaly
17p13.3 microduplication syndrome
Lissencephaly due to LIS1 mutation
Miller-Dieker syndrome
Subcortical band heterotopia
Narcolepsy-cataplexy
Anotia
Bilateral microtia - deafness - cleft palate
Complete androgen insensitivity syndrome
Familial hypospadias
Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies
Idiopathic central precocious puberty
Kennedy disease
Microtia
Papillary or follicular thyroid carcinoma
Partial androgen insensitivity syndrome
Distal 22q11.2 microdeletion syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
NDE1 Q9NXR1609449
No signs/symptoms info available.