| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Coloboma (D003103) |
Parent Node:
Growth Disorders (D006130) |
Parent Node:
Intellectual Disability (D008607) |
Parent Node:
Polydactyly (D017689) |
..Starting node
.. Pfeiffer Mayer syndrome (C537888)
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Child Nodes:
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Sister Nodes: |
..Absence of tibia with polydactyly (C535564)
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..Biemond Syndrome II (C565902)
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..Biemond syndrome type 2 (C535439)
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..Brachyphalangy, polydactyly, and tibial aplasia/hypoplasia (C537100)
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..Cortical Blindness, Retardation, and Postaxial Polydactyly (C565674)
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..Crossed Polydactyly, Type I (C566783)
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..Dandy Walker malformation postaxial polydactyly (C535771)
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..Desbuquois syndrome (C535943)
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..Ectodermal dysplasia alopecia preaxial polydactyly (C538016)
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..Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet (C565067)
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..Garret Tripp syndrome (C535646)
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..Hirschsprung disease polydactyly heart disease (C538120)
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..Hirschsprung Disease with Heart Defects, Laryngeal Anomalies, and Preaxial Polydactyly (C565817)
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..Hirschsprung Disease with Polydactyly, Renal Agenesis, and Deafness (C565518)
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..Hirschsprung Disease with Ulnar Polydactyly, Polysyndactyly of Big Toes, and Ventricular Septal Defect (C565517)
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..Holoprosencephaly 9 (C563659)
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..Hydrolethalus Syndrome 1 (C565504)
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..Kozlowski-Krajewska syndrome (C537615)
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..Laurence Prosser Rocker syndrome (C537882)
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..Liver Fibrocystic Disease and Polydactyly (C565272)
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..Maroteaux Fonfria syndrome (C536023)
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..McKusick Kaufman syndrome (C538159)
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..Meckel Syndrome, Type 4 (C567003)
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..Meckel-Like Cerebrorenodigital Syndrome (C567004)
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..Megalanecephaly Polymicrogyria-Polydactyly Hydrocephalus Syndrome (C566381)
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..Mexican Cardiomelic Dysplasia (C563087)
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..Oliver Syndrome (C564931)
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..Pallister-Hall Syndrome (D054975)
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..Pfeiffer Mayer syndrome (C537888)
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..Polydactyly myopia syndrome (C536331)
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..Polydactyly preaxial type 1 (C536332)
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..Polydactyly, Postaxial (C562429)
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..Polydactyly, Postaxial, Type A2 (C566585)
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..Polydactyly, Postaxial, Type A3 (C564590)
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..Polydactyly, Postaxial, Type A4 (C563909)
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..Polydactyly, Postaxial, with Dental and Vertebral Anomalies (C564880)
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..Polydactyly, preaxial 4 (C536333)
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..POLYDACTYLY, PREAXIAL II (OMIM:174500)
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..Polydactyly, Preaxial III (C566784)
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..Polysyndactyly, Crossed (C566773)
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..Preaxial deficiency, postaxial polydactyly and hypospadias (C538278)
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..Preaxial Hallucal Polydactyly (C566632)
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..Pseudotrisomy 13 syndrome (C535829)
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..Santos Mateus Leal syndrome (C537235)
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..Santos Syndrome (C567819)
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..Scalp defects postaxial polydactyly (C536622)
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..Short Rib-Polydactyly Syndrome (D012779)  3
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..SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY (OMIM:613091)
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..Syndactyly, Type IV (C566092)
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..Syndactyly-Polydactyly-Earlobe Syndrome (C566091)
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..Synpolydactyly 2 (C564278)
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..Synpolydactyly 3 (C565216)
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..Synpolydactyly With Foot Anomalies (C566095)
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..Thai Symphalangism Syndrome (C564303)
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..Tibia absent polydactyly arachnoid cyst (C536918)
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..Tibia, Absence or Hypoplasia of, with Polydactyly, Retrocerebellar Arachnoid Cyst, and Other Anomalies (C563403)
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..Tibia, Hypoplasia of, with Polydactyly (C566046)
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..Ulnar Ray Dysgenesis with Postaxial Polydactyly and Renal Cystic Dysplasia (C565783)
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..Urioste Martinez-Frias syndrome (C536478)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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