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Familial multiple meningioma
1 OMIM reference -
5 associated genes
192 connected diseases
No signs/symptoms info
Disease Type of connection
Coffin-Siris syndrome
Familial rhabdoid tumor
Bilateral striopallidodentate calcinosis
Atypical teratoid tumor
Neurofibromatosis type 3
Dermatofibrosarcoma protuberans
Desmoplastic / nodular medulloblastoma
Medulloblastoma with extensive nodularity
Intellectual deficit - sparse hair - brachydactyly
Precursor B-cell acute lymphoblastic leukemia
Idiopathic hypereosinophilic syndrome
Atypical Rett syndrome
Intellectual deficit, X-linked - psychosis - macroorchidism
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Trisomy Xq28
X-linked non-syndromic intellectual deficit
Precursor T-cell acute lymphoblastic leukemia
B-cell chronic lymphocytic leukemia
Congenital dyserythropoietic anemia type IV
Estrogen resistance syndrome
Hereditary persistence of fetal hemoglobin - beta-thalassemia
Hereditary persistence of fetal hemoglobin - sickle cell disease
6q25 microdeletion syndrome
Essential thrombocythemia
Acute basophilic leukemia
Beta-thalassemia - X-linked thrombocytopenia
Congenital erythropoietic porphyria
Thrombocytopenia with congenital dyserythropoietic anemia
Williams syndrome
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
Ehlers-Danlos syndrome type 1
Ehlers-Danlos / osteogenesis imperfecta syndrome
High bone mass osteogenesis imperfecta
Osteogenesis imperfecta type 1
Osteogenesis imperfecta type 2
Osteogenesis imperfecta type 3
Osteogenesis imperfecta type 4
Familial pancreatic carcinoma
Autosomal recessive primary microcephaly
Translocation renal cell carcinoma
Glucocorticoid resistance
Isolated adermatoglyphia
Pseudohypoaldosteronism type 2E
Gastrointestinal stromal tumor
Myeloid neoplasm associated with PDGFRA rearrangement
Burkitt lymphoma
Adrenocortical carcinoma
Chronic myelomonocytic leukemia
Giant cell glioblastoma
Infantile myofibromatosis
Li-Fraumeni syndrome
Myeloid neoplasm associated with PDGFRB rearrangement
Papilloma of choroid plexus
Synovial sarcoma
Unclassified chronic myeloproliferative disease
Dyssegmental dysplasia, Silverman-Handmaker type
Schwartz-Jampel syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Baraitser-Winter syndrome
Developmental malformations - deafness - dystonia
Neonatal diabetes - congenital hypothyroidism - congenital glaucoma - hepatic fibrosis - polycystic kidneys
Caffey disease
Ehlers-Danlos syndrome type 7A
Ehlers-Danlos syndrome, vascular-like type
Infantile Refsum disease
Neonatal adrenoleukodystrophy
Zellweger syndrome
Acrocallosal syndrome
Alobar holoprosencephaly
Alveolar soft-part sarcoma
Combined pituitary hormone deficiencies, genetic forms
Greig cephalopolysyndactyly syndrome
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Pallister-Hall syndrome
Polysyndactyly, bilateral
Polysyndactyly, unilateral
Postaxial polydactyly type A, bilateral
Postaxial polydactyly type A, unilateral
Postaxial polydactyly type B, bilateral
Postaxial polydactyly type B, unilateral
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Tyrosinemia type 2
Xeroderma pigmentosum complementation group C
Anophthalmia / microphthalmia - esophageal atresia
CHARGE syndrome
Colobomatous microphthalmia
Isolated anophthalmia - microphthalmia
Kallmann syndrome
Normosmic congenital hypogonadotropic hypogonadism
Omenn syndrome
Septo-optic dysplasia
Ataxia-telangiectasia variant
Combined cervical dystonia
Mantle cell lymphoma
Squamous cell carcinoma of head and neck
Amyotrophic lateral sclerosis
Cowden syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Proteus syndrome
Achondrogenesis type 2
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures
Autosomal dominant rhegmatogenous retinal detachment
Bethlem myopathy
Congenital muscular dystrophy, Ullrich type
Czech dysplasia, metatarsal type
Ehlers-Danlos syndrome type 2
Ehlers-Danlos syndrome type 7B
Ehlers-Danlos syndrome, cardiac valvular type
Ehlers-Danlos syndrome, vascular type
Familial abdominal aortic aneurysm
Familial avascular necrosis of femoral head
Familial cerebral saccular aneurysm
Familial porencephaly
Familial vascular leukoencephalopathy
Kniest dysplasia
Legg-Calvé-Perthes disease
Mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis
Multiple epiphyseal dysplasia, Beighton type
Otospondylomegaepiphyseal dysplasia
Platyspondylic dysplasia, Torrance type
Premature chromosome condensation with microcephaly and intellectual deficit
Spondyloepimetaphyseal dysplasia congenita, Strudwick type
Spondyloepiphyseal dysplasia congenita
Spondylometaphyseal dysplasia, 'corner fracture' type
Spondylometaphyseal dysplasia, Schmidt type
Spondyloperipheral dysplasia - short ulna
Stickler syndrome type 1
Syndromic multisystem autoimmune disease due to Itch deficiency
Walker-Warburg syndrome
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Split hand-split foot malformation
46,XY partial gonadal dysgenesis
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Adams-Oliver syndrome
Autosomal dominant secondary polycythemia
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Cardiomyopathy - hypotonia - lactic acidosis
Childhood-onset nemaline myopathy
Chronic myeloid leukemia
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Dedifferentiated liposarcoma
Familial platelet syndrome with predisposition to acute myelogenous leukemia
Intermediate nemaline myopathy
Isolated delta-storage pool disease
Multiple paragangliomas associated with polycythemia
Myelofibrosis with myeloid metaplasia
Nestor-Guillermo progeria syndrome
Pancytopenia due to IKZF1 mutations
Papillary or follicular thyroid carcinoma
Severe congenital nemaline myopathy
Sporadic pheochromocytoma
Sporadic secreting paraganglioma
Typical nemaline myopathy
Well-differentiated liposarcoma
X-linked Emery-Dreifuss muscular dystrophy
Acute promyelocytic leukemia
Early-onset autosomal dominant Alzheimer disease
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
Familial prostate cancer
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Costello syndrome
Familial retinoblastoma
Linear nevus sebaceus syndrome
Monosomy 13q14
Phakomatosis pigmentokeratotica
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Unilateral retinoblastoma
Richieri Costa-Pereira syndrome
(no synonyms)

Classification (Orphanet):
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.