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Pilocytic astrocytoma
7 associated genes
176 connected diseases
No signs/symptoms info
Disease Type of connection
Noonan syndrome
Cardiofaciocutaneous syndrome
LEOPARD syndrome
Kallmann syndrome
Costello syndrome
Linear nevus sebaceus syndrome
Normosmic congenital hypogonadotropic hypogonadism
Juvenile myelomonocytic leukemia
Hereditary nonpolyposis colon cancer
Familial pancreatic carcinoma
Hairy cell leukemia
Hashimoto-Pritzker syndrome
Giant cell glioblastoma
Hartsfield-Bixler-Demyer syndrome
Isolated trigonocephaly
Myeloid neoplasm associated with FGFR1 rearrangement
Osteoglophonic dwarfism
Pfeiffer syndrome type 1
Septo-optic dysplasia
Distal 22q11.2 microdeletion syndrome
Cowden syndrome
Follicular lymphoma
Intravascular large B-cell lymphoma
Autoimmune lymphoproliferative syndrome
Phakomatosis pigmentokeratotica
Noonan syndrome-like disorder with loose anagen hair
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Proteus syndrome
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Catecholaminergic polymorphic ventricular tachycardia
Amyotrophic lateral sclerosis
Autosomal agammaglobulinemia
SHORT syndrome
X-linked non-syndromic intellectual deficit
Autosomal dominant hypohidrotic ectodermal dysplasia
Autosomal dominant nonsyndromic intellectual deficit
Autosomal dominant spastic paraplegia type 13
Pelizaeus-Merzbacher-like due to HSPD1 mutation
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Large congenital melanocytic nevus
Familial retinoblastoma
Monosomy 13q14
Unilateral retinoblastoma
Burkitt lymphoma
Ondine syndrome
Precursor T-cell acute lymphoblastic leukemia
WAGR syndrome
X-linked lymphoproliferative disease
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Idiopathic hypereosinophilic syndrome
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRB rearrangement
Unclassified chronic myeloproliferative disease
Glucocorticoid resistance
Severe combined immunodeficiency due to LCK deficiency
Cerebellar ataxia - hypogonadism
Coffin-Lowry syndrome
Distal 16p11.2 microdeletion syndrome
Hereditary spherocytosis
MALT lymphoma
Proximal 16p11.2 microdeletion syndrome
Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
Testicular non seminomatous germ cell tumor
Testicular seminomatous germ cell tumor
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
Williams syndrome
CLOVE syndrome
Distal myopathy, Nonaka type
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Complete androgen insensitivity syndrome
Familial hypospadias
Kennedy disease
Partial androgen insensitivity syndrome
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Immunodeficiency by defective expression of HLA class 2
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Bleeding diathesis due to thromboxane synthesis deficiency
2q23.1 microdeletion syndrome
Acute promyelocytic leukemia
Adult-onset distal myopathy due to VCP mutation
Autosomal dominant hyper-IgE syndrome
Autosomal dominant hypophosphatemic rickets
Autosomal dominant secondary polycythemia
Autosomal recessive epidermolysis bullosa simplex
B-cell chronic lymphocytic leukemia
Behavioral variant of frontotemporal dementia
Carbamoylphosphate synthetase deficiency
Coffin-Siris syndrome
Desmoid tumor
Familial drusen
Familial gastric cancer
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Familial rhabdoid tumor
Familial thoracic aortic aneurysm and aortic dissection
Gastric linitis plastica
Generalized pseudohypoaldosteronism type 1
Glycogen storage disease due to liver phosphorylase kinase deficiency
Hepatocellular carcinoma, childhood-onset
Hereditary sensory and autonomic neuropathy type 6
Hermansky-Pudlak syndrome type 7
Herpetic encephalitis
Huntington disease
Hypercalcemic tumoral calcinosis
Hyperparathyroidism - jaw tumor syndrome
Idiopathic bronchiectasis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Intellectual deficit, X-linked, Turner type
Jawad syndrome
Juvenile Huntington disease
Leber congenital amaurosis
Lethal congenital contracture syndrome type 2
Liddle syndrome
Microvillous inclusion disease
Parathyroid carcinoma
Progressive non-fluent aphasia
Rare isolated myopia
Retinitis pigmentosa
Seckel syndrome
Semantic dementia
Spastic paraplegia - Paget disease of bone
Spinocerebellar ataxia type 12
Split hand-split foot malformation
Steinert myotonic dystrophy
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
Alobar holoprosencephaly
Lobar holoprosencephaly
Microform holoprosencephaly
Midline interhemispheric variant of holoprosencephaly
Multiple synostoses syndrome
Nodulosis-arthropathy-osteolysis syndrome
Renal tubular dysgenesis of genetic origin
Semilobar holoprosencephaly
Septopreoptic holoprosencephaly
Torg-Winchester syndrome
Autosomal recessive systemic lupus erythematosus
Common variable immunodeficiency
Deafness with labyrinthine aplasia, microtia, and microdontia
Hereditary gingival fibromatosis
Hyperinsulinism due to INSR deficiency
Insulin-resistance syndrome type A
Juvenile rheumatoid factor-negative polyarthritis
Oculootodental syndrome
Oligoarticular juvenile arthritis
Otodental syndrome
Primary mediastinal large B-cell lymphoma
Rabson-Mendenhall syndrome
Autosomal recessive lymphoproliferative disease
(no synonyms)

Classification (Orphanet):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.