Phenotypes for disease #04144 (OFD14 (orofaciodigital syndrome, type XIV (OFD-14)), OMIM:615948)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000129036 Occipital encephalocele (HP:0002085), bifid tongue (HP:0010297), sloping forehead (HP:0000340), microretrognathia (HP:0000308), ventricular septal defect (HP:0001629), hypoplastic thyroid (HP:0005990) - - Familial, autosomal recessive <00y - - - - Nicole Boczek 00163924
0000129037 molar tooth sign (HP:0002419), global developmental delay (HP:0001263), lobulated tongue (HP:0000180), micrognathia (HP:0000347), retinal coloboma (HP:0000480), posteriorly rotated ears (HP:0000358), intrauterine growth restriction (HP:0001511), hypotonia (HP:0001290) - - Familial, autosomal recessive - - <00y - - Nicole Boczek 00163925
0000129100 facial dysmorphism, cleft tongue, lobulated tongue, buccal frenulae, lingual hamartoma, cleft palate, absent epiglottis, supernumary teeth, bilaterail hand post axial polydactyly, bilateral broad hallux; microcephaly (OFC 42.3cm, -5 SD); no ataxia, no abnormal eye movements, no nystagmus, no ventilatory disorders (apnea, hyperpnea), no deafness, retinopathy, intellectual disability; walking, no speech; molar tooth signs; incomplete corpus callosum agenesis, subarachnoid cysts, myelinisation defect, no cardiac malformations, no abdominorenal malformations; micropenis; sister similar anomalies and cardiac malformation leading to neonatal death orofaciodigital syndrome OFD-14 Familial, autosomal recessive 04y - - - - Johan den Dunnen 00163997
0000129101 fetus 22w gestation; facial dysmorphism, no cleft tongue, no lobulated tongue, buccal frenulae, no lingual hamartoma, no cleft palate, no absent epiglottis, bilaterail hand post axial polydactyly, bilateral broad hallux; microcephaly (brain weight 50g, -4 SD); vermian hypoplasia; incomplete corpus callosum agenesis, subarachnoid cysts, no myelinisation defect, no cardiac malformations; right renal hypoplasia; micropenis - - Familial, autosomal recessive - - - - - Johan den Dunnen 00163998
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