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2 OMIM references -
1 associated gene
24 signs/symptoms
PROTEIN INTERACTIONS: 1
6 OMIM references -
2 associated genes
No signs/symptoms info
Stiff skin syndrome
Juvenile glaucoma

FBN1 CYP1B1
MYOC


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FBN1
(0.75)
MYOC



Citations in the biomedical literature:


Stiff skin syndrome
FBN1
Juvenile glaucoma
CYP1B1 MYOC



Stiff skin syndrome
Juvenile glaucoma

Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

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

Stiff skin syndrome

Very frequent
- Autosomal dominant inheritance
- Dermal / subcutaneous infiltration / induration
- Restricted joint mobility / joint stiffness / ankylosis
- Thick skin / pachydermia / orange skin
- Tight skin / lack of elasticity

Occasional
- Abnormal fat distribution / lipodystrophy
- Chronic arterial hypertension
- Glaucoma
- Hyperlipidemia / hypercholesterolemia / hypertriglyceridemia
- Insensitivity to pain
- Insulin-independent / type 2 diabetes
- Lipoatrophy
- Mid-facial hypoplasia / short / small midface
- Muscle anomalies
- Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy
- Muscle weakness / flaccidity
- Peripheral neuropathy
- Retinal detachment
- Sensorineural deafness / hearing loss
- Short stature / dwarfism / nanism
- Skin hypoplasia / aplasia / atrophy
- Strabismus / squint
- Subcutaneous nodules / lipomas / tumefaction / swelling
- Urinary / renal lithiasis / kidney stones / nephritic colic


Juvenile glaucoma

(no data available)