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46,XY gonadal dysgenesis - motor and sensory neuropathy
1 OMIM reference -
1 associated gene
10 connected diseases
No signs/symptoms info
Disease Type of connection
46,XY complete gonadal dysgenesis
Commissural facial cleft
Alobar holoprosencephaly
Gorlin syndrome
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Monosomy 9q22.3
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
(no synonyms)

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare gynecologic or obstetric disease
- Rare urogenital disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
DHH O43323605423
No signs/symptoms info available.