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1 OMIM reference -
1 associated gene
26 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1
3 OMIM references -
4 associated genes
45 signs/symptoms
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Berardinelli-Seip congenital lipodystrophy

HDAC6 AGPAT2
BSCL2
CAV1
FOS


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HDAC6
(0.49)
CAV1



Citations in the biomedical literature:


X-linked dominant chondrodysplasia, Chassaing-Lacombe type
HDAC6
Berardinelli-Seip congenital lipodystrophy
AGPAT2 BSCL2 CAV1 FOS



X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Berardinelli-Seip congenital lipodystrophy

Synonym(s):
- X-linked dominant chondrodysplasia - hydrocephaly - microphthalmia

Synonym(s):
- BSCL
- Beradinelli-Seip syndrome
- Brunzell syndrome
- GCL
- Generalized congenital lipodystrophy
- Lipoatrophic diabetes

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

Classification (ICD10):
(no data available)
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: -
Type of inheritance: x-linked dominant
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
No MeSH references


COMMON
SIGNS
- Intellectual deficit / mental / psychomotor retardation / learning disability


X-linked dominant chondrodysplasia, Chassaing-Lacombe type
Berardinelli-Seip congenital lipodystrophy

Very frequent
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- Dysostosis / chondrodysplasia / osteodysplasia / osteochondrosis / skeletal dysplasia
- Flattened nose
- Frontal bossing / prominent forehead
- Hydrocephaly
- Low set ears / posteriorly rotated ears
- Metacarpal anomalies / Archibald's sign
- Pelvis anomaly / Narrow / broad iliac wings / pubis abnormality
- Platyspondyly
- Rhizomelic micromelia
- Short foot / brachydactyly of toes
- Short hand / brachydactyly
- Short stature / dwarfism / nanism
- Short / small nose
- X-linked dominant inheritance

Frequent
- Ankle anomalies
- Asymmetry of the body / hemiatrophy / hemihyperthrophy
- Death in infancy
- Intrauterine growth retardation
- Rib structure anomalies

Occasional
- Cerebellum / cerebellar vermis anomaly / agenesis / hypoplasia
- Hyperkeratosis / ainhum / hyperkeratotic skin fissures
- Macrostomia / big mouth
- Micrognathia / retrognathia / micrognathism / retrognathism
- Short philtrum


Very frequent
- Abnormal fat distribution / lipodystrophy
- Acanthosis nigricans
- Advanced bone age
- Autosomal recessive inheritance
- Broad foot
- Diabetes mellitus
- Foot anomalies
- Hepatomegaly / liver enlargement (excluding storage disease)
- Hyperinsulinism / hyperinsulinemia
- Hyperlipidemia / hypercholesterolemia / hypertriglyceridemia
- Insulin resistance
- Large hand
- Lipoatrophy
- Muscle hypertrophy
- Prognathism / prognathia
- Prominent supraorbital ridge
- Storage liver disease
- Thick skin / pachydermia / orange skin

Frequent
- Abnormal pigmentary skin changes / skin pigmentation anomalies
- Acromegaly
- Bone cyst
- Cardiomyopathy / hypertrophic / dilated
- Hair and scalp anomalies
- Hepatocellular liver disease / hepatic failure
- Hirsutism / hypertrichosis / Increased body hair
- Hyperhidrosis / increased sweating
- Precocious puberty

Occasional
- Abnormal / polycystic ovaries
- Angor pectoris / myocardial infarction
- Anomalies of tongue, gingiva and oral mucosa
- Arterial stenosis / occlusion
- Cirrhosis
- Dilated cerebral ventricles without hydrocephaly
- Early death / lethality
- Immunodeficiency / increased susceptibility to infections / recurrent infections
- Liver / hepatic steatosis
- Metrorrhagia / menorrhagia / hemorrhagic cycles / hyper / poly / spanio / dysmenorrhea
- Mutiple fractures / bone fragility
- Pancreatitis
- Peripheral neuropathy
- Pulmonary hypertension
- Renal disease / nephropathy
- Renal failure
- Renal glomerular defect / glomerulopathy