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1 OMIM reference -
2 associated genes
10 signs/symptoms
PROTEIN INTERACTIONS: 1
3 OMIM references -
2 associated genes
No signs/symptoms info
Lethal acantholytic epidermolysis bullosa
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

DSP MUC1
JUP UMOD


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
JUP
(0.85)
MUC1



Citations in the biomedical literature:


Lethal acantholytic epidermolysis bullosa
DSP JUP
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia
MUC1 UMOD



Lethal acantholytic epidermolysis bullosa
Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

Synonym(s):
- LAEB

Synonym(s):
- Autosomal dominant nephronophthisis

Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
(no data available)

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C535493
External references:
3 OMIM references -
No MeSH references

Lethal acantholytic epidermolysis bullosa

Very frequent
- Absent / small fingernails / anonychia of hands
- Alopecia
- Autosomal recessive inheritance
- Chronic skin infection / ulcerations / ulcers / cancrum
- Early death / lethality
- Enanthema / aphtosa / aphta / leukoplakia
- Premature eruption of teeth / natal teeth
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment

Occasional
- Cardiomyopathy / hypertrophic / dilated
- Epigastralgia / heartburn / gastric / duodenal ulcer / gastritis


Autosomal dominant medullary cystic kidney disease with or without hyperuricemia

(no data available)