Cytoscape Web
Click node...


1 OMIM reference -
2 associated genes
10 signs/symptoms
PROTEIN INTERACTIONS: 2
1 OMIM reference -
1 associated gene
No signs/symptoms info
Lethal acantholytic epidermolysis bullosa
Isolated growth hormone deficiency type II

DSP GH1
JUP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
JUP
(0.63)
(0.63)
GH1
GH1



Citations in the biomedical literature:


Lethal acantholytic epidermolysis bullosa
DSP JUP
Isolated growth hormone deficiency type II
GH1



Lethal acantholytic epidermolysis bullosa
Isolated growth hormone deficiency type II

Synonym(s):
- LAEB

Synonym(s):
- Congenital IGHD type II
- Congenital isolated GH deficiency type II
- Congenital isolated growth hormone deficiency type II

Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

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: -
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
1 MeSH reference: C535493
External references:
1 OMIM reference -
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


Isolated growth hormone deficiency type II

(no data available)