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Bladder exstrophy
1 OMIM reference -
1 associated gene
81 connected diseases
14 signs/symptoms
Disease Type of connection
Split hand-split foot malformation
ADULT syndrome
Ankyloblepharon - ectodermal defects - cleft lip / palate
EEC syndrome
Limb-mammary syndrome
Familial pancreatic carcinoma
Precursor B-cell acute lymphoblastic leukemia
Amyotrophic lateral sclerosis
46,XY partial gonadal dysgenesis
Adrenocortical carcinoma
B-cell chronic lymphocytic leukemia
Essential thrombocythemia
Giant cell glioblastoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Syndromic multisystem autoimmune disease due to Itch deficiency
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
Uveal coloboma - cleft lip and palate - intellectual deficit
Frontotemporal dementia with motor neuron disease
Juvenile amyotrophic lateral sclerosis
Myxoid / round cell liposarcoma
2q32q33 microdeletion syndrome
2q33.1 microdeletion syndrome
Adult-onset distal myopathy due to VCP mutation
Autosomal recessive spastic ataxia of Charlevoix-Saguenay
Behavioral variant of frontotemporal dementia
Distal myopathy with posterior leg and anterior hand involvement
Dowling-Degos disease
Epidermolysis bullosa simplex with circinate migratory erythema
Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex, Dowling-Meara type
Epidermolytic palmoplantar keratoderma
Familial isolated congenital asplenia
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Isolated ATP synthase deficiency
Localized epidermolysis bullosa simplex
Muscle filaminopathy
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Translocation renal cell carcinoma
X-linked osteoporosis with fractures
Acute promyelocytic leukemia
Familial melanoma
Melanoma and neural system tumor syndrome
Melanoma-pancreatic cancer syndrome
Precursor T-cell acute lymphoblastic leukemia
Anaplastic ependymoma
Aneurysm - osteoarthritis syndrome
Autism spectrum disorder-epilepsy-arthrogryposis syndrome
Autoimmune lymphoproliferative syndrome
Autosomal dominant limb-girdle muscular dystrophy type 1D
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Autosomal recessive limb-girdle muscular dystrophy type 2S
Autosomal recessive primary microcephaly
Ear-patella-short stature syndrome
Ewing sarcoma
Familial prostate cancer
Familial thoracic aortic aneurysm and aortic dissection
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Intellectual disability-hyperkinetic movement-truncal ataxia syndrome
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Peutz-Jeghers syndrome
Primary peritoneal carcinoma
Denys-Drash syndrome
Desmoplastic small round cell tumor
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Frasier syndrome
Meacham syndrome
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
WAGR syndrome
- Classic exstrophy of the bladder

Classification (Orphanet):
- Rare abdominal surgical disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare renal disease
- Rare urogenital disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -

Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: multigenic/multifactorial
External references:
1 OMIM reference -
1 MeSH reference: D001746

Gene symbol UniProt reference OMIM reference
TP63 Q9H3D4603273
Very frequent
- Anus / rectum anomalies
- Bladder / cloacal exstrophy
- Clitoris / labia majora / labia minora / female external genitalia hypoplasia
- Hypospadias / epispadias / bent penis
- Micropenis / small penis / agenesis
- Umbilical hernia
- Vesicorenal / vesicoureteral reflux

- Inguinal / inguinoscrotal / crural hernia
- Recurrent urinary infections
- Urethral anomalies / stenosis / posterior urethral valves / megalocystis

- Encopresis / fecal incontinence
- Intestinal / gut / bowel malrotation
- Omphalocele / exomphalos
- Short bowel