Cytoscape Web
Click node...


1 OMIM reference -
2 associated genes
10 signs/symptoms
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
24 signs/symptoms
Lethal acantholytic epidermolysis bullosa
Pitt-Hopkins syndrome

DSP TCF4
JUP


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
JUP
(0.55)
TCF4



Citations in the biomedical literature:


Lethal acantholytic epidermolysis bullosa
DSP JUP
Pitt-Hopkins syndrome
TCF4



Lethal acantholytic epidermolysis bullosa
Pitt-Hopkins syndrome

Synonym(s):
- LAEB

Synonym(s):
(no synonyms)

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

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 / 1 000 000
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 -
1 MeSH reference: C537403

Lethal acantholytic epidermolysis bullosa
Pitt-Hopkins syndrome

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


Very frequent
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Anteverted nares / nostrils
- Ataxia / incoordination / trouble of the equilibrium
- Autosomal dominant inheritance
- Constipation
- Deepset eyes / enophthalmos
- Failure to thrive / difficulties for feeding in infancy / growth delay
- Gastroesophageal reflux / pyrosis / esophagitis / hiatal hernia / gastroparesia
- Helix thickened / sculpted
- Hypotonia
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Macrostomia / big mouth
- Microcephaly
- Palate anomalies
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
- Thick lips

Frequent
- Apnea / sleep apnea
- Myopia
- Respiratory rhythm disorder
- Seizures / epilepsy / absences / spasms / status epilepticus
- Tapered fingers
- Undescended / ectopic testes / cryptorchidia / unfixed testes

Occasional
- Irregular / patchy skin hypopigmentation
- Micropenis / small penis / agenesis