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Isolated adermatoglyphia
1 OMIM reference -
1 associated gene
29 connected diseases
No signs/symptoms info
Disease Type of connection
Coffin-Siris syndrome
Precursor T-cell acute lymphoblastic leukemia
Constitutional mismatch repair deficiency syndrome
Cornelia de Lange syndrome
Familial multiple meningioma
Familial rhabdoid tumor
Hereditary nonpolyposis colon cancer
Muir-Torre syndrome
Non-polyposis Turcot syndrome
Acute promyelocytic leukemia
Adult-onset autosomal dominant leukodystrophy
Atypical teratoid tumor
Burkitt lymphoma
Cataract - intellectual deficit - hypogonadism
Distal myopathy with vocal cord weakness
Distal myopathy, Nonaka type
Extraskeletal Ewing sarcoma
Familial isolated dilated cardiomyopathy
Hereditary breast and ovarian cancer syndrome
Kleefstra syndrome due to 9q34 microdeletion
Kleefstra syndrome due to a point mutation
Micro syndrome
Neuroblastoma
Neurofibromatosis type 3
Nijmegen breakage syndrome-like disorder
Severe combined immunodeficiency due to DNA-PKcs deficiency
Sialuria
Translocation renal cell carcinoma
Williams syndrome
Synonym(s):
- Absence of fingerprints
- Immigration delay disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SMARCAD1 Q9H4L7612761
No signs/symptoms info available.