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2 OMIM references -
2 associated genes
14 signs/symptoms
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Autosomal dominant cutis laxa
Hereditary sensorimotor neuropathy with hyperelastic skin

ELN FBLN5
FBLN5


COMMON
GENES
FBLN5


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ELN
(0.76)
FBLN5



Citations in the biomedical literature:


Autosomal dominant cutis laxa
ELN FBLN5
Hereditary sensorimotor neuropathy with hyperelastic skin



Autosomal dominant cutis laxa
Hereditary sensorimotor neuropathy with hyperelastic skin

Synonym(s):
- ADCL

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare skin disease
- Rare surgical thoracic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
2 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references

Autosomal dominant cutis laxa

Very frequent
- Autosomal dominant inheritance
- Loose skin / skin relaxation / excess skin / creases

Frequent
- Abnormal fat distribution / lipodystrophy
- Broad cheeks / cherub-like / cherubin face
- Colonic / intestinal / bowel diverticulosis / diverticulitis
- Hyperextensible joints / articular hyperlaxity
- Hypertelorism
- Premature ageing

Occasional
- Aortic valve anomaly / incompetence / insufficiency / regurgitation / bicuspid
- Cardiac valvulopathy
- Emphysema
- Herniae
- Inguinal / inguinoscrotal / crural hernia
- Pulmonary valve atresia / stenosis / narrowing


Hereditary sensorimotor neuropathy with hyperelastic skin

(no data available)