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1,670 Possible Causes for Multiple Crown Malformations, Small Foot

  • Rothmund Thomson Syndrome

    They include a wide variety of malformations such as microdontia, rudimentary or hypoplastic teeth, multiple and unusual crown formations, and disorders of dental breakthrough[] […] eyeball 0000568 Osteoporosis 0000939 Short foot Short feet Small feet [ more ] 0001773 Short nose Decreased length of nose Shortened nose [ more ] 0003196 Short palm 0004279[] Short thumb Short thumbs Small thumbs [ more ] 0009778 Small hand Disproportionately small hands 0200055 Strabismus Cross-eyed Squint Squint eyes [ more ] 0000486 Talipes[]

  • Early Infantile Epileptic Encephalopathy Type 2

    Forms and Documents Test Details Genes: Expand Genes ADSL, ALDH5A1, ALDH7A1, ALG13, ARHGEF9, ARX, ASNS, ATP1A2, ATP1A3, ATP6AP2, ATRX, BRAT1, CACNA1A, CASK, CDKL5, CHD2, CHRNA2, CHRNA4, CHRNA7, CHRNB2, CLCN4, CLN3, CLN5, CLN6, CLN8, CNTNAP2, CSTB, CTNNB1, CTSD, CTSF, DDX3X, DEPDC5, DNAJC5, DNM1, DYRK1A, EEF1A2, EHMT1,[…][]

    Missing: Multiple Crown Malformations
  • Cardiodysrhythmic Potassium-Sensitive Periodic Paralysis

    Andersen's syndrome is a clinically distinct form of potassium-sensitive periodic paralysis associated with cardiac dysrhythmias. The subtle nature of the cardiac and dysmorphic features may delay the recognition of this syndrome and its potentially lethal cardiac dysrhythmias. The genetic defect in Andersen's[…][]

    Missing: Multiple Crown Malformations
  • Rett Syndrome

    Rett Syndrome NORD gratefully acknowledges Jeffrey L. Neul, MD, PhD, Chief of Division of Child Neurology, University of California, San Diego and Rady Children’s Hospital San Diego, for assistance in the preparation of this report. Synonyms of Rett Syndrome classic Rett syndrome RTT variant (atypical) Rett syndrome[…][]

    Missing: Multiple Crown Malformations
  • Autosomal Recessive Spastic Paraplegia Type 20

    When present it is found in distal muscles in the lower limbs, usually the small muscles of the foot and tibialis anterior.[]

    Missing: Multiple Crown Malformations
  • Sanjad-Sakati Syndrome

    foot - Small hand / acromicria - Thin / retracted lips Frequent - Anomalies of teeth and dentition - Enamel anomaly - Repeat respiratory infections Occasional - Anophthalmos[] (very frequent sign) seizures (any type) (very frequent sign) short stature/dwarfism (very frequent sign) small foot (very frequent sign) small hand (very frequent sign) thin[] Microcephaly - Micrognathia / retrognathia / micrognathism / retrognathism - Seizures / epilepsy / absences / spasms / status epilepticus - Short stature / dwarfism / nanism - Small[]

    Missing: Multiple Crown Malformations
  • Kenny-Caffey Syndrome Type 1

    ; Short palm ; Slender long bone ; Small hand ; Tetany ; Thin clavicles ; Thin ribs Associated Genes TBCE (Withdrawn symbols: HRD, KCS, KCS1, pac2 ) Mouse Orthologs Tbce[] […] delay as children 0008897 Short foot Short feet Small feet [ more ] 0001773 Small hand Disproportionately small hands 0200055 Stenosis of the medullary cavity of the long[] Hypertelorism ; Hypocalcemia ; Hypomagnesemia ; Intrauterine growth retardation ; Long clavicles ; Proportionate short stature ; Recurrent bacterial infections ; Seizures ; Short foot[]

    Missing: Multiple Crown Malformations
  • Acrootoocular Syndrome

    Disease definition A very rare disorder associating pseudopapilledema (optic disc swelling not secondary to increased intracranial pressure), mixed hearing loss, facial dysmorphism and limb extremity anomalies. Summary Epidemiology Only 4 cases have been reported in the literature from 3 inbred sibships. Clinical[…][]

    Missing: Multiple Crown Malformations
  • Prader-Willi Syndrome

    The Hebrew University's Prof. Nissim Benvenisty. Credit: Hebrew University (Medical Xpress)—Scientists at the Hebrew University of Jerusalem have reported a major breakthrough in understanding the molecular basis for Prader-Willi syndrome (PWS), perhaps the most studied among the class of diseases that involves[…][]

    Missing: Multiple Crown Malformations
  • X-Linked Syndromic Mental Retardation Type Armfield

    Genes and mapped phenotypes Gene ID: 57791, updated on 8-Apr-2017 Summary Gene symbol MRXSA Gene description Armfield X-linked mental retardation syndrome Primary source MIM:300261 Gene type unknown Organism Homo sapiens Lineage Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;[…][]

    Missing: Multiple Crown Malformations

Further symptoms