Phenotypes for disease #05160 (MOHR;OFD2 (MOHR syndrome (MOHR, orofaciodigital syndrome type 2 (OFD-2))), OMIM:252100)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000050834 incomplete midline lip, alveolar cleft (HP:0010289), submucous cleft hard palate (HP:0000176), bifid tongue with hyperplastic frenula, tongue hamartomas, general dental hypoplasia (HP:0006282), dental agenesis (HP:0000674), central incisors and cuspids with talon cusps, taurodontia (HP:0000679), maxillary hypoplasia (HP:0010650), brachydactyly, syndactyly of fingers, bilateral broad hallux, mild mesomeric limb shortening in lower limbs, mild conductivehearing loss, bilateral tortuosity of the retinal veins (HP:0012841) - - Familial, autosomal recessive - - - - - Glen Monroe 00064296
0000050835 incomplete midline lip, alveolar cleft (HP:0010289), Submucous cleft hard palate (HP:0000176), hyperplastic frenula, tongue hamartomas, general dental hypoplasia (HP:0006282), dental agenesis (HP:0000674), cupular shaped upper incisors, taurodontia (HP:0000679), maxillary hypoplasia (HP:0010650), protruding ears (HP:0000411), brachydactyly, clinodactyly digiti V (HP:0004209), bifid right hallux, broad left hallux, mild mesomeric limb shortening in lower limbs, progressive (mainly conductive) hearing loss (HP:0005101), bilateral tortuosity of the retinal veins (HP:0012841) - - Familial, autosomal recessive - - - - - Glen Monroe 00064295
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.