Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Total intestinal aganglionosis |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital enlargement of coronary sinus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macrodactyly of toes - fatty nerve tumor |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of sphenoid bone |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macrogyria |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of nasal cavity |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Fallot's triad |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of pulmonary valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of cardiac ventricle |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital tracheobronchomegaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Tsuge operation on finger for macrodactyly repair |
Direct morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macrodactyly of toe (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of testis |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Unilateral congenital macrostomia |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of tricuspid valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Giant esophagus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital onychauxis |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital macrostomia |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Giant kidney |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital splenomegaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of aortic valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Megaloappendix |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of adrenal gland |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of lung |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital syphilitic splenomegaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macrogenia |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital thickening of ulna |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macrotia |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital enlargement of nasopharynx |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Familial megalencephaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Bannayan syndrome |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Repair of macrodactyly |
Direct morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Bilateral congenital macrostomia |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macroencephaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Sporadic megalencephaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital macrognathism |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macrodactyly of toes - simple |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of ovary |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of pylorus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Macrophthalmos |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Hirschsprung's disease NOS |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital aganglionic megacolon |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Repair of macrodactyly of finger |
Direct morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of mitral valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Fetal macrocephaly (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of fallopian tube (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of fallopian tube (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Aganglionosis of Auerbach's plexus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Fetal macrocephaly (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Hemimegalencephaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Fallot's trilogy |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Hemimegalencephaly |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Fallot's trilogy |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of adrenal gland |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Fallot's trilogy |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
4 |
Congenital hypertrophy of ovary |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of cardiac ventricle |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Myostatin related hypertrophy of muscle |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of pulmonary valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of lung |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of fallopian tube (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of aortic valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of cardiac ventricle |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of pylorus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of retinal pigment epithelium |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of adrenal gland |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of nasal cavity |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital hypertrophy of mitral valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of ovary |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital hypertrophy of testis |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital hypertrophy of ureteric valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of tricuspid valve |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Congenital hypertrophy of sphenoid bone |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Giant esophagus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Mowat-Wilson syndrome (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
4 |
Long segment Hirschsprung's disease |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
4 |
Short segment Hirschsprung's disease |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
4 |
Congenital aganglionic megacolon |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
4 |
Total intestinal aganglionosis |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
4 |
Mowat-Wilson syndrome (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Aganglionosis of Auerbach's plexus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
5 |
Congenital overgrowth of partial lower limb |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital overgrowth of foot |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital overgrowth of whole lower limb |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital overgrowth of lower limb |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital overgrowth of proximal lower limb |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital overgrowth of distal lower limb |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Congenital macrocheilia |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Congenital macrodactyly (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
2 |
Waardenburg-Shah syndrome (WSS), also known as Waardenburg syndrome type 4 (WS4) is characterized by the association of Waardenburg syndrome (sensorineural hearing loss and pigmentary abnormalities) and Hirschsprung disease (aganglionic megacolon). |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
7 |
Haddad syndrome is a rare congenital disorder in which congenital central hypoventilation syndrome (CCHS), or Ondine syndrome, occurs concurrently with Hirschsprung disease. |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
6 |
Hirschsprung disease-type D brachydactyly syndrome is characterized by Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two maternal uncles). Transmission appears to be X-linked recessive but autosomal dominant inheritance with incomplete penetrance in females cannot be ruled out. |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
7 |
Hirschsprung disease-nail hypoplasia-dysmorphism syndrome is a fatal malformative disorder that is characterised by Hirschsprung disease, hypoplastic nails, distal limb hypoplasia and minor craniofacial dysmorphic features (flat facies, upward slanting palpebral fissures, narrow philtrum, narrow, high arched palate, micrognathia, low set ears with abnormal helices). Hydronephrosis has also been reported. There have been no further descriptions in the literature since 1988. |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
10 |
Hirschsprung disease-deafness-polydactyly syndrome is an extremely rare malformative association, described in only two siblings to date, characterized by Hirschsprung disease (defined by the presence of an aganglionic segment of variable extent in the terminal part of the colon that leads to symptoms of intestinal obstruction, including constipation and abdominal distension), polydactyly of hands and/or feet, unilateral renal agenesis, hypertelorism and congenital deafness. There have been no further descriptions in the literature since 1988. |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
9 |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by Hirschsprung disease, facial dysmorphism (sloping forehead, high arched eyebrows, long eyelashes, telecanthus/hypertelorism, ptosis, prominent ears, thick earlobes, prominent nasal bridge, thick philtrum, everted lower lip vermillion and pointed chin), global developmental delay, intellectual disability and variable cerebral abnormalities (focal or generalized polymicrogyria, or hypoplastic corpus callosum). |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
10 |
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome is characterized by precocious obesity, congenital hypothyroidism, neonatal colitis, cardiac hypertrophy, craniosynostosis and developmental delay. It has been described in two brothers, one of whom died within the first month of life. The parents of the two children were nonconsanguineous and in good health, however, the pregnancies were complicated by a maternal HELLP syndrome (Haemolysis, Elevated Liver enzymes and Low Platelets). The mode of inheritance has not yet been clearly established. |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
9 |
Waardenburg-Shah syndrome (WSS), also known as Waardenburg syndrome type 4 (WS4) is characterized by the association of Waardenburg syndrome (sensorineural hearing loss and pigmentary abnormalities) and Hirschsprung disease (aganglionic megacolon). |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
1 |
Aganglionosis of Auerbach's plexus |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Mowat-Wilson syndrome (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
3 |
Hirschsprung disease of rectosigmoid region (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
6 |
Extensive aganglionosis Hirschsprung disease (disorder) |
Associated morphology |
False |
hypertrophie congénitale |
Inferred relationship |
Some |
4 |