| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Family history of congenital microcephaly |
constatation associée (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
1 |
| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Amish lethal microcephaly (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Achalasia microcephaly syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Stimmler syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| 3-phosphoglycerate dehydrogenase deficiency infantile form (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Autosomal recessive chorioretinopathy and microcephaly syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Anonychia with microcephaly syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Aphalangy and syndactyly with microcephaly syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Autosomal dominant primary microcephaly |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Cleft palate, large ears, small head syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| syndrome de pseudo-infection intra-utérine congénitale |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Cutaneous mastocytosis, short stature, hearing loss syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Autosomal recessive primary microcephaly (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| syndrome d'extrasystoles, petite taille, hyperpigmentation, microcéphalie |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Goldberg Shprintzen megacolon syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Filippi syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Hydromicrocephaly |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| syndrome d'hypogonadisme hypogonadotrope-microcéphalie sévère-surdité neurosensorielle-dysmorphie |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Hall Riggs syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| syndrome de Jawad |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Intellectual disability, feeding difficulties, developmental delay, microcephaly syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| syndrome d'agénésie du corps calleux-microcéphalie-petite taille |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic primordial dwarfism Alazami type (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic primordial dwarfism Dauber type |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Lowry MacLean syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic osteodysplastic primordial dwarfism types I and III (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic primordial dwarfism Montreal type |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus cardiomyopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus cleft palate syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic primordial dwarfism of Toriello type (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Hadziselimovic syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus co-occurrent with cervical spine fusion anomaly (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| microcéphalie-microcornée type Seemanova |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus with albinism and digital anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus with cardiac defect and lung malsegmentation syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus, complex motor and sensory axonal neuropathy syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus, glomerulonephritis, marfanoid habitus syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephaly with deafness and intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalus, lymphedema, chorioretinopathy syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephaly with simplified gyral pattern |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephaly, seizure, intellectual disability, heart disease syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephaly-capillary malformation syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Neu-Laxova syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Nijmegen breakage syndrome-like disorder (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Oculocerebrofacial syndrome Kaufman type (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Oro-facial digital syndrome type 14 |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Oculopalatocerebral syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Prominent glabella with microcephaly and hypogenitalism syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| nanisme à tête d'oiseau |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Pseudoprogeria syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Severe X-linked intellectual disability Gustavson type (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic osteodysplastic primordial dwarfism type II |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
| 19p13.3 microduplication syndrome (disorder) |
est un(e) (attribut) |
True |
Congenital microcephaly (disorder) |
Inferred relationship |
Some |
|
FHIR