Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Aglossia-adactyly syndrome |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of digits NOS |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of thumb |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of finger |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of toe |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ectrodactyly (disorder) |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Partial aphalangia of upper limb |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Anonychia |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aphalangy and syndactyly with microcephaly syndrome (disorder) |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Robin sequence and oligodactyly syndrome (disorder) |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intellectual disability, spasticity, ectrodactyly syndrome |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare, genetic, multiple congenital anomalies syndrome characterised by variable expression of the holoprosencephaly (HPE) spectrum in association with ectrodactyly, cleft lip/palate and/or other ectodermal anomalies. Developmental delay of variable severity and endocrine abnormalities are often associated. |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Split hand, split foot malformation with sensorineural hearing loss syndrome |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aplasia of fibula and ectrodactyly syndrome (disorder) |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ectrodactyly polydactyly syndrome (disorder) |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acro-dermato-ungual-lacrimal-tooth syndrome (disorder) |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder) |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transverse deficiency of toe |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of great toe |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of fifth toe |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Partial aphalangia of lower limb (disorder) |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of multiple toes |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Complete aphalangia of lower limb (disorder) |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
An exceedingly rare, autosomal recessive immune disease characterised by thumb aplasia, short stature with skeletal abnormalities, and combined immunodeficiency described in three sibships from two possibly related families. The skeletal abnormalities included unfused olecranon and the immunodeficiency manifested with severe chickenpox and chronic candidiasis. No new cases have been reported since 1978. |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Complete aphalangia of upper limb |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital absence of all bilateral toes |
Is a |
False |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Tetramelic monodactyly (disorder) |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Agenesis of epiphysis of phalanx of toe (disorder) |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Aplasia of phalanx of hand |
Is a |
True |
Adactyly |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|