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

MUC1 DSP
UMOD JUP


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


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



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

Synonym(s):
- Autosomal dominant nephronophthisis

Synonym(s):
- LAEB

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

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

Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
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

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

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)