External genital hypoplasia
Symptom Information:
Symptom ID: | HPO:0003241 | |||||
Synonyms: |
|
|||||
Quality: | ||||||
Cross references: |
|
|||||
Is a (Direct Parents): |
|
|||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormal external genitalia(HPO:0000811) External genital hypoplasia(HPO:0003241) MedDRA: |
|||||
Database Frequency: | 25 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
Bardet-Biedl syndrome 1 | (OMIM:209900 ) |
Bardet-Biedl syndrome 10 | (OMIM:615987) |
Bardet-Biedl syndrome 13 | (OMIM:615990) |
Bardet-Biedl syndrome 16 | (OMIM:615993) |
Bardet-Biedl syndrome 19 | (OMIM:615996) |
Bardet-Biedl syndrome 2 | (OMIM:615981) |
Bardet-Biedl syndrome 3 | (OMIM:600151) |
Bardet-Biedl syndrome 5 | (OMIM:615983) |
Bardet-Biedl syndrome 6 | (OMIM:605231) |
Bardet-Biedl syndrome 7 | (OMIM:615984) |
Bardet-Biedl syndrome 8 | (OMIM:615985) |
Carpenter syndrome | (Orphanet:65759) |
FANCONI ANEMIA, COMPLEMENTATION GROUP O | (OMIM:613390) |
Harrod syndrome | (Orphanet:2115) |
MESOAXIAL HEXADACTYLY AND CARDIAC MALFORMATION | (OMIM:249670) |
MICROCEPHALY, GROWTH RETARDATION, CATARACT, HEARING LOSS, AND UNUSUALAPPEARANCE | (OMIM:612947) |
Meckel syndrome | (Orphanet:564) |
Meckel syndrome, type 1 | (OMIM:249000) |
Micro syndrome | (Orphanet:2510) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
RETINITIS PIGMENTOSA INVERSA WITH DEAFNESS | (OMIM:268010) |
Self-healing collodion baby | (Orphanet:281122) |
Short stature - craniofacial anomalies - genital hypoplasia | (Orphanet:2994) |
TESTES, RUDIMENTARY | (OMIM:273150) |
WARBURG MICRO SYNDROME 1 | (OMIM:600118) |