Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Poikiloderma, alopecia, retrognathism, cleft palate syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hidrotic ectodermal dysplasia Christianson Fourie type (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Pilodental dysplasia, refractive errors syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Digital extensor muscle aplasia with polyneuropathy (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Ptosis and vocal cord paralysis syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Absent radius, anogenital anomalies syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Teebi Shaltout syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Torticollis, keloids, cryptorchidism, renal dysplasia syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Cleft palate, large ears, small head syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Grubben, De Cock, Borghgraef syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Conductive deafness, ptosis, skeletal anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Facial dysmorphism, conductive hearing loss, heart defect syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Congenital myopathy with myasthenic-like onset (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Connective tissue disorder due to lysyl hydroxylase-3 deficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Cerebrofacioarticular syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial progressive hyper and hypopigmentation |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Velofacioskeletal syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Wiedemann Steiner syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
White forelock with malformations syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Craniodigital syndrome and intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spastic ataxia with congenital miosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Curly hair, acral keratoderma, caries syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial vesicoureteral reflux (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hypotonia, speech impairment, severe cognitive delay syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Isolated congenital adermatoglyphia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Dislocation of hip and facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Macrocephaly and developmental delay syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Keipert syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Malan overgrowth syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Agenesis of corpus callosum and abnormal genitalia syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Microcephalus, complex motor and sensory axonal neuropathy syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Oculoauricular syndrome Schorderet type |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Oro-facial digital syndrome type 1 (disorder) |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Oro-facial digital syndrome type 14 |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Neonatal Marfan syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Pachygyria, intellectual disability, epilepsy syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Postaxial polydactyly, anterior pituitary anomalies, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia Handigodu type |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Short stature with delayed bone age due to thyroid hormone metabolism deficiency (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Renal hepatic pancreatic dysplasia (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Brachydactyly elbow wrist dysplasia (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Retinal arterial macroaneurysm with supravalvular pulmonic stenosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia anauxetic type (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial isolated trichomegaly |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Branchiootic syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Congenital myopathy with internal nuclei and atypical cores (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
King Denborough syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, myopathy, short stature, endocrine defect syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial thoracic aortic aneurysm and aortic dissection |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Nail and tooth abnormalities, marginal palmoplantar keratoderma, oral hyperpigmentation syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Rolandic epilepsy, speech dyspraxia syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial generalised lentiginosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Dyssegmental dysplasia Silverman Handmaker type (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hartsfield syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
X-linked cleft palate and ankyloglossia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Radio-renal syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Trichodysplasia xeroderma syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Trichoodontoonychial dysplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Short stature due to growth hormone secretagogue receptor deficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia with multiple dislocations |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia, short limb, abnormal calcification syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Diencephalic mesencephalic junction dysplasia (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Cono-spondylar dysplasia (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Multicentric carpotarsal osteolysis syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Severe neonatal onset encephalopathy with microcephaly (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Ectodermal dysplasia syndactyly syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Polymicrogyria with optic nerve hypoplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Parietal foramina with clavicular hypoplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Jawad syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Thrombocythemia with distal limb defect (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autism spectrum disorder due to AUTS2 deficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Facial dysmorphism, immunodeficiency, livedo, short stature syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
RAB18, member RAS oncogene family deficiency (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
X-linked intellectual disability, craniofacioskeletal syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Postaxial polydactyly, dental, vertebral anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Thakker Donnai syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Macrosomia, microphthalmia, cleft palate syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia, hypotrichosis syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondyloepimetaphyseal dysplasia Genevieve type (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Zechi Ceide syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
CK syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Craniosynostosis and dental anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive frontotemporal pachygyria (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Roifman syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability with strabismus syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Mandibular hypoplasia, deafness, progeroid syndrome (disorder) |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|