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1 OMIM reference -
1 associated gene
6 signs/symptoms
PROTEIN INTERACTIONS: 1
COMMON SIGNS: 3
3 OMIM references -
4 associated genes
25 signs/symptoms
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Pachyonychia congenita

DSP KRT16
KRT17
KRT6A
KRT6B


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
DSP
(0.55)
KRT6A



Citations in the biomedical literature:


Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
DSP
Pachyonychia congenita
KRT16 KRT17 KRT6A KRT6B



Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Pachyonychia congenita

Synonym(s):
- Carvajal syndrome
- Woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome
- Wooly hair - palmoplantar keratoderma - dilated cardiomyopathy
- Wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome

Synonym(s):
- PC

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

Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

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

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D053549


COMMON
SIGNS
- Autosomal recessive inheritance
- Palmoplantar hyperkeratosis / keratoderma
- Vesicles / bullous / exsudative lesions / bullous / cutaneous / mucosal detachment


Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
Pachyonychia congenita

Very frequent
- Cardiomyopathy / hypertrophic / dilated
- Woolly / frizzy hair

Occasional
- Heart / cardiac failure


Very frequent
- Abnormal nails colour / leukonychia / melanonychia
- Autosomal dominant inheritance
- Dysplastic / thick / grooved fingernails
- Dysplastic / thick / grooved toenails
- Enanthema / aphtosa / aphta / leukoplakia
- Hair and scalp anomalies
- Hyperhidrosis / increased sweating
- Nails anomalies

Frequent
- Absent / small fingernails / anonychia of hands
- Anomalies of teeth and dentition
- Ichthyosis / ichthyosiform dermatitis
- Multiple caries
- Skin tumors / lumps / epidermal cysts

Occasional
- Abnormal fingernails
- Alopecia
- Cataract / lens opacification
- Corneal dystrophy
- Hepatomegaly / liver enlargement (excluding storage disease)
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Laryngomalacia
- Respiratory distress / dyspnea / respiratory failure / lung volume reduction