Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Intellectual disability, facial dysmorphism, hand anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Xylosyltransferase 1 congenital disorder of glycosylation |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Severe intellectual disability, short stature, behavioural abnormalities, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Severe intellectual disability, poor language, strabismus, grimacing face, long fingers syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
THO complex 6-related developmental delay, microcephaly, facial dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Short ulna, dysmorphism, hypotonia, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondylocostal dysostosis, hypospadias, intellectual disability syndrome |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, craniofacial dysmorphism, cryptorchidism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Aphonia, deafness, retinal dystrophy, bifid halluces, intellectual disability syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Muscular hypertrophy, hepatomegaly, polyhydramnios syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Chudley McCullough syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, hypotonia, brachycephaly, pyloric stenosis, cryptorchidism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Craniofacial dysplasia osteopenia syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Short stature, onychodysplasia, facial dysmorphism, hypotrichosis syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Porencephaly, microcephaly, bilateral congenital cataract syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Multiple congenital anomalies, hypotonia, seizures syndrome type 2 |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Progeroid and marfanoid aspect, lipodystrophy syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial infantile gigantism |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract, hearing loss, severe developmental delay syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Distal Xq28 microduplication syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Lethal occipital encephalocele, skeletal dysplasia syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hypoplasia of pancreas, intestinal atresia, hypoplasia of gallbladder syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Spondylo-megaepiphyseal-metaphyseal dysplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Pitt Hopkins-like syndrome |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Leukonychia totalis, acanthosis-nigricans-like lesions, abnormal hair syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Sterile multifocal osteomyelitis with periostitis and pustulosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Deafness with onychodystrophy syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
NPHP3-related Meckel-like syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Genitopalatocardiac syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Flat face, microstomia, ear anomaly syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Emery Nelson syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Ataxia, photosensitivity, short stature syndrome |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Rare non-syndromic intellectual disability |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Piebald trait with neurologic defects syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Peripheral dysostosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
AHDC1-related intellectual disability, obstructive sleep apnoea, mild dysmorphism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
FBLN1-related developmental delay, central nervous system anomaly, syndactyly syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Pancytopenia with developmental delay syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, obesity, prognathism, eye and skin anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Sacral agenesis, abnormal ossification of vertebral bodies, persistent notochordal canal syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Short stature, auditory canal atresia, mandibular hypoplasia, skeletal anomalies syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Growth retardation, mild developmental delay, chronic hepatitis syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Severe dermatitis, multiple allergies, metabolic wasting syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Trichorhinophalangeal syndrome type 1 and 3 |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hereditary elliptocytosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Mullerian aplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal dominant familial woolly hair |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive familial woolly hair |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Macular corneal dystrophy |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Erythrokeratodermia variabilis |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Moynahan syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Focal facial dermal dysplasia type I |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Focal facial dermal dysplasia type II |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Focal facial dermal dysplasia type IV |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Blue cone monochromatism |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Short-limb skeletal dysplasia with severe combined immunodeficiency |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Woodhouse Sakati syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Periventricular nodular heterotopia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial penile hypospadias |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive asexual dwarfism |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
X-linked asexual dwarfism |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hereditary camptodactyly |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Antley-Bixler syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Recessive aplasia cutis congenita of limbs |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal dominant hypophosphataemic bone disease |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
17q23.1-q23.2 duplication syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Coralliform cataract |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Acrocardiofacial syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Bilateral frontoparietal polymicrogyria |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Megalencephaly capillary malformation |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Brachydactyly type D |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Brachydactyly type A3 |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal dominant polycystic liver disease |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Jackson-Weiss syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Saethre-Chotzen syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Familial spinal neurofibromatosis |
Is a |
False |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Type 3 lissencephaly |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Genochondromatosis type 1 |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Osteogenesis imperfecta type 5 |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
X-linked congenital generalised hypertrichosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Wrinkly skin syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Fibrous skin tumour of tuberous sclerosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Pulmonary tuberous sclerosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Ash leaf spot, tuberous sclerosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
17q11 deletion syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Intestinal epithelial dysplasia |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Amish lethal microcephaly |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|
Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts |
Is a |
True |
Developmental hereditary disorder |
Inferred relationship |
Some |
|