Cytoscape Web
Click node...

Familial porencephaly
2 OMIM references -
2 associated genes
44 connected diseases
No signs/symptoms info
Disease Type of connection
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
Familial vascular leukoencephalopathy
Schizencephaly
Walker-Warburg syndrome
Chuvash erythrocytosis
Von Hippel-Lindau disease
Early-onset autosomal dominant Alzheimer disease
Fibronectin glomerulopathy
Granular corneal dystrophy type I
Granular corneal dystrophy type II
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Lattice corneal dystrophy type I
Metaphyseal anadysplasia
Microcystic corneal dystrophy
Reis-Bücklers corneal dystrophy
Thiel-Behnke corneal dystrophy
Acral dystrophic epidermolysis bullosa
Centripetalis recessive dystrophic epidermolysis bullosa
Dystrophic epidermolysis bullosa pruriginosa
Dystrophic epidermolysis bullosa, nails only
Epidermolysis bullosa simplex superficialis
Generalized dominant dystrophic epidermolysis bullosa
Pretibial dystrophic epidermolysis bullosa
Recessive dystrophic epidermolysis bullosa inversa
Recessive dystrophic epidermolysis bullosa-generalized other
Severe generalized recessive dystrophic epidermolysis bullosa
Transient bullous dermolysis of the newborn
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Ménière disease
Bilateral striopallidodentate calcinosis
Dermatofibrosarcoma protuberans
Familial multiple meningioma
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Congenital stromal corneal dystrophy
Infantile systemic hyalinosis
Juvenile hyaline fibromatosis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
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: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
1 MeSH reference: C536850
Gene symbol UniProt reference OMIM reference
COL4A1 P02462120130
COL4A2 P08572120090
No signs/symptoms info available.