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Fetal and neonatal alloimmune thrombocytopenia
6 associated genes
106 connected diseases
No signs/symptoms info
Disease Type of connection
Bernard-Soulier syndrome
Autosomal dominant macrothrombocytopenia
Glanzmann thrombasthenia
22q11.2 deletion syndrome
Von Willebrand disease, platelet type
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
Atelosteogenesis type I
Atelosteogenesis type III
Autosomal dominant Larsen syndrome
Boomerang dysplasia
Spondylocarpotarsal synostosis
Von Willebrand disease type 1
Von Willebrand disease type 2A
Von Willebrand disease type 2B
Von Willebrand disease type 2M
Von Willebrand disease type 2N
Von Willebrand disease type 3
Ehlers-Danlos syndrome type 7B
Ehlers-Danlos syndrome, cardiac valvular type
Cerebral sinovenous thrombosis
Congenital factor II deficiency
Familial afibrinogenemia
Familial dysfibrinogenemia
Familial hypodysfibrinogenemia
Familial hypofibrinogenemia
Idiopathic hypereosinophilic syndrome
Chronic intestinal pseudoobstruction
Congenital short bowel syndrome
Congenital valvular dysplasia
Ehlers-Danlos syndrome with periventricular heterotopia
Frontometaphyseal dysplasia
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Periventricular nodular heterotopia
Terminal osseous dysplasia - pigmentary defects
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
Severe generalized recessive dystrophic epidermolysis bullosa
Achondrogenesis type 2
Autosomal dominant rhegmatogenous retinal detachment
Congenital factor XII deficiency
Czech dysplasia, metatarsal type
Familial avascular necrosis of femoral head
Hereditary angioedema type 3
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
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
Congenital factor XI deficiency
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Gastrointestinal stromal tumor
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRA rearrangement
Myeloid neoplasm associated with PDGFRB rearrangement
Precursor B-cell acute lymphoblastic leukemia
Unclassified chronic myeloproliferative disease
Atypical hemolytic uremic syndrome with MCP / CD46 anomaly
Congenital analbuminemia
Caffey disease
Dermatofibrosarcoma protuberans
Ehlers-Danlos syndrome type 1
Ehlers-Danlos syndrome type 7A
Ehlers-Danlos syndrome, vascular-like type
Chronic granulomatous disease
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Familial isolated dilated cardiomyopathy
Juvenile myelomonocytic leukemia
LEOPARD syndrome
Miller-Dieker syndrome
Myxoid / round cell liposarcoma
Noonan syndrome
Posterior polar cataract
Total congenital cataract
Fibronectin glomerulopathy
Congenital high-molecular-weight kininogen deficiency
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Cowden syndrome
Dyssegmental dysplasia, Silverman-Handmaker type
Essential thrombocythemia
Familial capillary hemangioma
Intermediate nemaline myopathy
Myelofibrosis with myeloid metaplasia
Proteus syndrome
Schwartz-Jampel syndrome
Severe congenital nemaline myopathy
Typical nemaline myopathy

Classification (Orphanet):
- Rare hematologic disease

Classification (ICD10):
- Certain conditions originating in the perinatal period -

Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.