Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital undergrowth of foot |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Syndactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital abnormality of lower limb and pelvic girdle (disorder) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of foot |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Perodactylia |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A genetic syndrome with limb reduction defects characterized by skeletal abnormalities of the upper limbs and mild-to-severe congenital cardiac defects. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Anisomelia |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Phocomelia |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Multiple malformation syndrome with facial-limb defects as major feature |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Notomelus |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Dimelia |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Polydactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Brachydactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Partial congenital absence of limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of upper limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Longitudinal deficiency of limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Limb reduction-ichthyosis syndrome |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Absent finger |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Brachymegalodactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Splayleg in piglets |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Polymelia |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital abnormal shape of digit |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital ankylodactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of claw |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of paw |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital hyperextension of limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Macromelia |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital hyperflexion of limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital hypoplasia of paw |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital malposition of digit |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital malposition of paw |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital malrotation of limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Duplication of whole limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
croissance partielle d'un membre entier |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital malformation syndromes involving limbs |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Aglossia-adactyly syndrome |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Multiple pterygium syndrome |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Popliteal pterygium syndrome |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
membre atrophié |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Adactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Other congenital limb anomalies |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Reduction deformity of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital absence of limb NOS |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Amelia of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Ectromelia of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Hemimelia of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Phocomelia of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital amputation of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Longitudinal reduction deformity of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Other specified reduction deformities of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Brachymelia NOS |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Other duplication of limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Other overgrowth of limb NOS |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Other specified anomalies of unspecified limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of unspecified limb NOS |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
[X]Other reduction defects of unspecified limb(s) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
[X]Other specified congenital malformations of limb(s) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital absence of digits NOS |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Reduction deformity of unspecified limb NOS |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Anonychia (disorder) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Pachyonychia congenita syndrome |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital complete absence of limb |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Ectrodactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of lower limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital onychauxis |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Other congenital anomalies of lower leg |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital bony fusion of phalanges (disorder) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Geleophysic dysplasia |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of digit (disorder) |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of nail |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Other congenital anomalies of upper leg |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Jeune syndrome, also called asphyxiating thoracic dystrophy, is a short-rib dysplasia characterized by a narrow thorax, short limbs and radiological skeletal abnormalities including trident aspect of the acetabula and metaphyseal changes. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Constricting band of extremity (disorder) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandible (hypoglossia, aglossia, micrognathia, glossopalatine ankylosis, cleft palate, and gingival anomalies). |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital anomaly of blood vessel of limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital undergrowth of foot |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Ectrodactyly |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Congenital bony fusion of phalanges (disorder) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Partial congenital absence of limb |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Constricting band of extremity (disorder) |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A rare disorder characterized by the association of mullerian duct and distal limb anomalies. Females present with anomalies ranging from a vaginal septum to complete duplication of uterus and vagina, and males present with micropenis. The limb anomalies varied from postaxial polydactyly to severe upper limb hypoplasia with split hand. |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Micromelia |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A spectrum of congenital malformative disorders characterized by the co-occurrence of distal limb anomalies (usually bilateral cleft feet and/or hands) and renal defects (e.g. unilateral or bilateral agenesis), that can be associated with a variety of other anomalies such as those of genitourinary tract (genital anomalies, ureteral hypoplasias, vesicoureteral reflux), abdominal well defects, intestinal atresias, and lung malformations. Familial cases have been reported in which an autosomal recessive inheritance was suspected. |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Campomelia, Cumming type, is characterized by the association of limb defects and multivisceral anomalies. |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A form of acromelic dysplasia characterized by the distinctive radiological sign of angel-shaped middle phalanges, a typical metacarpophalangeal pattern profile (mainly affecting first metacarpals and middle phalanges of second, third and fifth digits, which all appear short), epiphyseal changes in the hips and, in some, abnormal dentition and delayed bone age. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Fuhrmann syndrome is mainly characterized by bowing of the femora, aplasia or hypoplasia of the fibulae and poly-, oligo-, and syndactyly. |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A rare multiple congenital anomalies syndrome characterized by the association of limb pterygia, heart anomalies, autosomal recessive inheritance, vertebral defects, ear anomalies and radial defects. |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Autosomal recessive aplasia cutis congenita of limb (disorder) |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A rare and severe inborn metabolic disease characterized clinically by the association of severe-to-profound neurodevelopmental impairment, severe visual impairment, ante-postnatal growth impairment, severe scoliosis and, frequently, early-onset epilepsy. |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A rare genetic disease characterized by the association of osteosarcoma with limb anomalies (such as bilateral radioulnar synostosis and clinodactyly, as well as other abnormalities of the hands and feet) and erythroid macrocytosis without anemia. There have been no further descriptions in the literature since 1977. |
Is a |
True |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
X-linked lethal multiple pterygium syndrome is a rare, genetic, developmental defect during embryogenesis characterized by the typical lethal multiple pterygium syndrome presentation (comprising of multiple pterygia, severe arthrogryposis, cleft palate, cystic hygromata and/or fetal hydrops, skeletal abnormalities and fetal death in the 2nd or 3rd trimester) with an X-linked pattern of inheritance. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome is a rare, genetic dysostosis syndrome, with marked inter- and intra-familial variation, typically characterized by triphalangeal thumbs, hand and/or foot polysyndactyly and/or absent/hypoplastic tibiae (associated with duplication of fibulae in some cases), although isolated triphalangeal thumbs have also been reported. It is often accompanied with remarkable short stature and additional features may include radio-ulnar synostosis and hand oligodactyly, as well as abnormal carpal and metatarsal bones. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Carney complex-trismus-pseudocamptodactyly syndrome is a rare genetic heart-hand syndrome characterized by typical manifestations of the Carney complex (spotty pigmentation of the skin, familial cardiac and cutaneous myxomas and endocrinopathy) associated with trismus and distal arthrogryposis (presenting as involuntary contraction of distal and proximal interphalangeal joints of hands evident only on dorsiflexion of wrist and similar lower-limb contractures producing foot deformities). |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Postaxial tetramelic oligodactyly is a rare, genetic, congenital limb malformation disorder characterized by isolated, postaxial oligodactyly in all four extremities. Patients present a consistent pattern of malformation ranging from complete absence of the 5th metacarpals, metatarsals and phalanges to complete absence of the 5th metacarpals and metatarsals, with some residual distal 5th phalanges. There have been no further descriptions in the literature since 1993. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Thrombocythemia with distal limb defects is a rare, genetic syndrome with limb reduction defects characterized by thrombocytosis, unilateral transverse limb defects (ranging from absence of phalanges to absence of hand or forearm) and splenomegaly. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A rare multiple congenital anomalies syndrome characterized by congenital microgastria and a uni- or bilateral limb reduction defect, that can include absent or hypoplastic thumbs, radius, ulna and/or amelia. Association with other variable abnormalities, including intestinal malrotation, asplenia, dysplastic kidneys, hypoplastic lungs, dysplastic corpus collosum, and abnormal genitalia, has been reported. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Ectromelia |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
Micromelic spondyloepimetaphyseal dysplasia |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|
A rare multiple congenital anomalies/dysmorphic syndrome characterized by skeletal dysplasia (including coronal clefting of the vertebral bodies and short limbs and variable congenital heart malformations, such as atrial and ventricular septal defects, right ventricular hypoplasia, and valve defects). There have been no further descriptions in the literature since 1990. |
Is a |
False |
Congenital anomaly of limb |
Inferred relationship |
Some |
|