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Polydactyly of a triphalangeal thumb, bilateral
2 associated genes
20 connected diseases
No signs/symptoms info
Disease Type of connection
Hypoplastic tibiae - postaxial polydactyly
Polydactyly of a triphalangeal thumb, unilateral
Radial hemimelia, bilateral
Radial hemimelia, unilateral
Syndactyly type 4
Triphalangeal thumb - polysyndactyly syndrome
Alobar holoprosencephaly
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Adactyly of foot, bilateral
Adactyly of foot, unilateral
Colobomatous microphthalmia
Schizencephaly
Solitary median maxillary central incisor syndrome
Gorlin syndrome
Monosomy 9q22.3
Commissural facial cleft
Synonym(s):
- Bilateral PPD2
- Preaxial polydactyly type 2, bilateral
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
LMBR1 Q8WVP7605522
SHH Q15465600725
No signs/symptoms info available.