Phenotype #0000299084
| Individual ID |
00394789 |
| Associated disease |
RRS |
| Phenotype details |
short stature; prominent forehead; hypertelorism; no proptosis; no long palpebral fissure; epicanthus; no strabismus; no upslanted palpebral; downslanted palpebral; no ptosis; no long eyelashes; midface retrusion; no depressed nasal bridge; wide nasal bridge; short nose; abnormality of the nasal tip; no anteverted nares; no long philtrum; no short philtrum; triangular mouth; no downturned corners of mouth; thin upper lip vermilion; gingival overgrowth; hypoplasia of tongue; bifid tongue; micrognathia; no retrognathia; no oral cleft; no melanocytic nevus; no microtia; low-set ears; short neck; no pectus excavatum; broad thumb; short palm; brachydactyly; no clinodactyly; nail dysplasia; no syndactyly; no camptodactyly; single transverse palmar crease; broad hallux; micropenis; no hypospadias; no cryptorchidism; no sacral dimple; no abnormal heart morphology; no abnormality of the kidney; no hearing impairment; no inguinal hernia; scoliosis; rib fusion; mesomelia; hemivertebrae; no limited pronation/supination of forearm; no hip dislocation |
| Diagnosis/Initial |
Robinow syndrome |
| Inheritance |
Familial, autosomal recessive |
| Diagnosis/Definite |
RRS1 |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-04-01 19:57:55 +02:00 (CEST) |
| Date last edited |
N/A |
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