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2 OMIM references -
2 associated genes
14 signs/symptoms
PROTEIN INTERACTIONS: 1
4 OMIM references -
3 associated genes
No signs/symptoms info
Autosomal dominant cutis laxa
Congenital glaucoma

ELN CYP1B1
FBLN5 LTBP2
MYOC


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FBLN5
(0.7)
LTBP2



Citations in the biomedical literature:


Autosomal dominant cutis laxa
ELN FBLN5
Congenital glaucoma
CYP1B1 LTBP2 MYOC



Autosomal dominant cutis laxa
Congenital glaucoma

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 developmental defect during embryogenesis
- Rare eye disease
- Rare genetic 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: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal recessive

External references:
2 OMIM references -
No MeSH references
External references:
4 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


Congenital glaucoma

(no data available)