Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hereditary camptodactyly (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dupuytren's disease of finger |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dupuytren's disease of palm (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fibromatosis colli |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dupuytren's disease of palm and finger(s), nodules with no contracture |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dupuytren's disease of palm and finger |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dupuytren's disease of finger, with contracture |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fibromatosis with contracture of plantar fascia |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dupuytren's contracture of finger |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Cherubism with gingival fibromatosis (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
maladie de Dupuytren |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Cross syndrome |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dupuytren's disease of palm and finger |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dupuytren's disease of palm and finger(s), nodules with no contracture |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dupuytren's disease of palm and finger, with contracture |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dupuytren's disease of palm and finger, with contracture |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Gingival fibromatosis |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Plantar fascial fibromatosis (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
maladie de Dupuytren |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Fibromatosis with contracture of plantar fascia |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
6 |
Gingival fibromatosis and hypertrichosis syndrome |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A very rare syndrome characterized by the association of gingival fibromatosis and craniofacial dysmorphism. |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Gingival fibromatosis with progressive deafness syndrome (disorder) |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Fibromatosis |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dupuytren's disease of palm of bilateral hands (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Dupuytren's disease of palm of left hand (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dupuytren's disease of palm of bilateral hands (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dupuytren's disease of palm of right hand (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Aggressive fibromatosis |
Is a |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cherubism with gingival fibromatosis (disorder) |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
A very rare disorder belonging to the heterogeneous group of genetic fibromatoses and with characteristics of progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid and adrenal glands. Caused by mutations in anthrax toxin receptor 2 gene (ANTRX2) on chromosome 4q21. Transmitted as an autosomal recessive trait. |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Infantile digital fibromatosis |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hyaline fibromatosis syndrome (disorder) |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Juvenile hyaline fibromatosis (disorder) |
Associated morphology |
False |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Sporadic camptodactyly |
Associated morphology |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Fibromatosis colli |
Is a |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Juvenile hyaline fibromatosis (morphologic abnormality) |
Is a |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Inclusion body fibromatosis |
Is a |
True |
Fibromatosis |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|